ENST00000371375.2:c.4303A>G
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ENSP00000360426.1:p.Thr1435Ala
|
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ENST00000685253.1:c.*1770A>G
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ENSP00000509405.1:n.*1770A>G
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ENST00000685889.1:n.1962A>G
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|
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ENST00000686807.1:n.646A>G
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|
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ENST00000686954.1:c.*511A>G
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ENSP00000508416.1:n.*511A>G
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ENST00000688810.1:c.4255A>G
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ENSP00000509140.1:p.Thr1419Ala
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ENST00000689233.1:n.9435A>G
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|
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ENST00000690340.1:n.2900A>G
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|
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ENST00000692286.1:c.5095A>G
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ENSP00000509490.1:p.Thr1699Ala
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ENST00000692396.1:c.5179A>G
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ENSP00000508605.1:p.Thr1727Ala
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ENST00000371380.8:c.5227A>G
MANE Select
|
ENSP00000360431.2:p.Thr1743Ala
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ENST00000371385.8:c.4201A>G
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ENSP00000360438.4:p.Thr1401Ala
|
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ENST00000674738.1:c.3782A>G
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|
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ENST00000674827.1:c.3343A>G
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ENSP00000502523.1:p.Thr1115Ala
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ENST00000675218.1:c.4303A>G
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ENSP00000501910.1:p.Thr1435Ala
|
|
ENST00000675487.1:c.*1160A>G
|
ENSP00000502340.1:n.*1160A>G
|
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ENST00000675718.1:c.4496A>G
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|
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ENST00000676102.1:c.4072A>G
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ENSP00000502811.1:p.Thr1358Ala
|
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ENST00000260766.7:c.5227A>G
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ENSP00000260766.3:p.Thr1743Ala
|
|
ENST00000371375.1:c.4303A>G
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ENSP00000360426.1:p.Thr1435Ala
|
|
ENST00000371380.7:c.5227A>G
|
ENSP00000360431.2:p.Thr1743Ala
|
|
ENST00000371385.7:c.4303A>G
|
ENSP00000360438.3:p.Thr1435Ala
|
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NM_001165979.2:c.4303A>G
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NP_001159451.1:p.Thr1435Ala
|
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NM_001288989.1:c.5179A>G
|
NP_001275918.1:p.Thr1727Ala
|
|
NM_016341.3:c.5227A>G
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NP_057425.3:p.Thr1743Ala
|
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XM_006717885.2:c.5269A>G
|
XP_006717948.1:p.Thr1757Ala
|
|
XM_006717886.2:c.5269A>G
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XP_006717949.1:p.Thr1757Ala
|
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XM_006717888.2:c.5266A>G
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XP_006717951.1:p.Thr1756Ala
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XM_006717889.2:c.5221A>G
|
XP_006717952.1:p.Thr1741Ala
|
|
XM_006717890.1:c.4345A>G
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XP_006717953.1:p.Thr1449Ala
|
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XM_011539849.1:c.5269A>G
|
XP_011538151.1:p.Thr1757Ala
|
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XM_011539850.1:c.4114A>G
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XP_011538152.1:p.Thr1372Ala
|
|
XM_006717885.4:c.5269A>G
|
XP_006717948.1:p.Thr1757Ala
|
|
XM_006717888.4:c.5266A>G
|
XP_006717951.1:p.Thr1756Ala
|
|
XM_006717889.4:c.5221A>G
|
XP_006717952.1:p.Thr1741Ala
|
|
XM_006717890.3:c.4345A>G
|
XP_006717953.1:p.Thr1449Ala
|
|
XM_011539849.3:c.5269A>G
|
XP_011538151.1:p.Thr1757Ala
|
|
XM_011539850.3:c.4114A>G
|
XP_011538152.1:p.Thr1372Ala
|
|
XM_017016310.2:c.5269A>G
|
XP_016871799.1:p.Thr1757Ala
|
|
XM_017016311.2:c.5269A>G
|
XP_016871800.1:p.Thr1757Ala
|
|
XM_017016312.2:c.4255A>G
|
XP_016871801.1:p.Thr1419Ala
|
|
NM_001288989.2:c.5179A>G
|
NP_001275918.1:p.Thr1727Ala
|
|
NM_016341.4:c.5227A>G
MANE Select
|
NP_057425.3:p.Thr1743Ala
|
|