ENST00000247933.9:c.1685G>C
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ENSP00000247933.4:p.Gly562Ala
|
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ENST00000514224.2:c.1685G>C
MANE Select
|
ENSP00000425081.2:p.Gly562Ala
|
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ENST00000652070.1:n.1741G>C
|
|
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ENST00000247933.8:c.1685G>C
|
ENSP00000247933.4:p.Gly562Ala
|
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ENST00000514224.1:c.1289G>C
|
ENSP00000425081.1:p.Gly430Ala
|
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ENST00000514417.1:n.77G>C
|
|
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ENST00000514698.5:n.1792G>C
|
|
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NM_000203.4:c.1685G>C
|
NP_000194.2:p.Gly562Ala
|
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NR_110313.1:n.1773G>C
|
|
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XM_006713882.2:c.1289G>C
|
XP_006713945.1:p.Gly430Ala
|
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XM_011513459.1:c.1751G>C
|
XP_011511761.1:p.Gly584Ala
|
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XM_011513460.1:c.1544G>C
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XP_011511762.1:p.Gly515Ala
|
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XM_011513461.1:c.1478G>C
|
XP_011511763.1:p.Gly493Ala
|
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XM_011513462.1:c.1397G>C
|
XP_011511764.1:p.Gly466Ala
|
|
XM_011513463.1:c.1397G>C
|
XP_011511765.1:p.Gly466Ala
|
|
XR_924947.1:n.1941G>C
|
|
|
NM_000203.5:c.1685G>C
MANE Select
|
NP_000194.2:p.Gly562Ala
|
|
NM_001363576.1:c.1289G>C
|
NP_001350505.1:p.Gly430Ala
|
|
XM_011513461.2:c.1478G>C
|
XP_011511763.1:p.Gly493Ala
|
|
XM_017008163.1:c.725G>C
|
XP_016863652.1:p.Gly242Ala
|
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