ENST00000339113.9:c.1667A>T
|
|
|
ENST00000378756.8:c.1703A>T
MANE Select
|
ENSP00000368031.3:p.Lys568Met
|
|
ENST00000400830.4:c.702A>T
|
|
|
ENST00000536055.6:c.1466A>T
|
ENSP00000439290.1:p.Lys489Met
|
|
ENST00000672388.1:n.2040A>T
|
|
|
ENST00000339113.8:c.1659A>T
|
|
|
ENST00000378755.9:c.1847A>T
|
ENSP00000368030.5:p.Lys616Met
|
|
ENST00000378756.7:c.1703A>T
|
ENSP00000368031.3:p.Lys568Met
|
|
ENST00000536055.5:c.1466A>T
|
ENSP00000439290.1:p.Lys489Met
|
|
NM_001170535.1:c.1703A>T
|
NP_001164006.1:p.Lys568Met
|
|
NM_001170536.1:c.1466A>T
|
NP_001164007.1:p.Lys489Met
|
|
NM_018188.3:c.1847A>T
|
NP_060658.3:p.Lys616Met
|
|
NM_001170535.2:c.1703A>T
|
NP_001164006.1:p.Lys568Met
|
|
NM_001170536.2:c.1466A>T
|
NP_001164007.1:p.Lys489Met
|
|
NM_018188.4:c.1847A>T
|
NP_060658.3:p.Lys616Met
|
|
XM_024448098.1:c.1781A>T
|
XP_024303866.1:p.Lys594Met
|
|
XR_001737282.1:n.1776A>T
|
|
|
XR_002956997.1:n.1854A>T
|
|
|
NM_001170535.3:c.1703A>T
MANE Select
|
NP_001164006.1:p.Lys568Met
|
|
NM_018188.5:c.1847A>T
|
NP_060658.3:p.Lys616Met
|
|
NM_001170536.3:c.1466A>T
|
NP_001164007.1:p.Lys489Met
|
|