ENST00000371375.2:c.4152A>G
|
ENSP00000360426.1:p.Lys1384=
|
|
ENST00000685253.1:c.*1619A>G
|
ENSP00000509405.1:n.*1619A>G
|
|
ENST00000685889.1:n.1811A>G
|
|
|
ENST00000686807.1:n.495A>G
|
|
|
ENST00000686954.1:c.*360A>G
|
ENSP00000508416.1:n.*360A>G
|
|
ENST00000688810.1:c.4104A>G
|
ENSP00000509140.1:p.Lys1368=
|
|
ENST00000689233.1:n.9284A>G
|
|
|
ENST00000690340.1:n.2749A>G
|
|
|
ENST00000692286.1:c.5036-4831A>G
|
ENSP00000509490.1:n.5036-4831A>G
|
|
ENST00000692396.1:c.5028A>G
|
ENSP00000508605.1:p.Lys1676=
|
|
ENST00000371380.8:c.5076A>G
MANE Select
|
ENSP00000360431.2:p.Lys1692=
|
|
ENST00000371385.8:c.4050A>G
|
ENSP00000360438.4:p.Lys1350=
|
|
ENST00000674738.1:c.3631A>G
|
|
|
ENST00000674827.1:c.3192A>G
|
ENSP00000502523.1:p.Lys1064=
|
|
ENST00000675218.1:c.4152A>G
|
ENSP00000501910.1:p.Lys1384=
|
|
ENST00000675487.1:c.*1009A>G
|
ENSP00000502340.1:n.*1009A>G
|
|
ENST00000675718.1:c.4345A>G
|
|
|
ENST00000676102.1:c.3921A>G
|
ENSP00000502811.1:p.Lys1307=
|
|
ENST00000260766.7:c.5076A>G
|
ENSP00000260766.3:p.Lys1692=
|
|
ENST00000371375.1:c.4152A>G
|
ENSP00000360426.1:p.Lys1384=
|
|
ENST00000371380.7:c.5076A>G
|
ENSP00000360431.2:p.Lys1692=
|
|
ENST00000371385.7:c.4152A>G
|
ENSP00000360438.3:p.Lys1384=
|
|
NM_001165979.2:c.4152A>G
|
NP_001159451.1:p.Lys1384=
|
|
NM_001288989.1:c.5028A>G
|
NP_001275918.1:p.Lys1676=
|
|
NM_016341.3:c.5076A>G
|
NP_057425.3:p.Lys1692=
|
|
XM_006717885.2:c.5118A>G
|
XP_006717948.1:p.Lys1706=
|
|
XM_006717886.2:c.5118A>G
|
XP_006717949.1:p.Lys1706=
|
|
XM_006717888.2:c.5115A>G
|
XP_006717951.1:p.Lys1705=
|
|
XM_006717889.2:c.5070A>G
|
XP_006717952.1:p.Lys1690=
|
|
XM_006717890.1:c.4194A>G
|
XP_006717953.1:p.Lys1398=
|
|
XM_011539849.1:c.5118A>G
|
XP_011538151.1:p.Lys1706=
|
|
XM_011539850.1:c.3963A>G
|
XP_011538152.1:p.Lys1321=
|
|
XM_006717885.4:c.5118A>G
|
XP_006717948.1:p.Lys1706=
|
|
XM_006717888.4:c.5115A>G
|
XP_006717951.1:p.Lys1705=
|
|
XM_006717889.4:c.5070A>G
|
XP_006717952.1:p.Lys1690=
|
|
XM_006717890.3:c.4194A>G
|
XP_006717953.1:p.Lys1398=
|
|
XM_011539849.3:c.5118A>G
|
XP_011538151.1:p.Lys1706=
|
|
XM_011539850.3:c.3963A>G
|
XP_011538152.1:p.Lys1321=
|
|
XM_017016310.2:c.5118A>G
|
XP_016871799.1:p.Lys1706=
|
|
XM_017016311.2:c.5118A>G
|
XP_016871800.1:p.Lys1706=
|
|
XM_017016312.2:c.4104A>G
|
XP_016871801.1:p.Lys1368=
|
|
NM_001288989.2:c.5028A>G
|
NP_001275918.1:p.Lys1676=
|
|
NM_016341.4:c.5076A>G
MANE Select
|
NP_057425.3:p.Lys1692=
|
|