ENST00000317961.9:c.3585G>A
MANE Select
|
ENSP00000322408.4:p.Trp1195Ter
|
|
ENST00000317961.8:c.3585G>A
|
ENSP00000322408.4:p.Trp1195Ter
|
|
ENST00000382806.6:c.3414G>A
|
ENSP00000372256.2:p.Trp1138Ter
|
|
ENST00000415360.1:c.501G>A
|
ENSP00000389433.1:p.Trp167Ter
|
|
ENST00000440077.5:c.3462G>A
|
ENSP00000398543.1:p.Trp1154Ter
|
|
ENST00000469599.6:n.2183G>A
|
|
|
ENST00000492117.1:n.3477G>A
|
|
|
ENST00000541639.5:c.3678G>A
|
ENSP00000444293.1:p.Trp1226Ter
|
|
NM_001146705.1:c.3678G>A
|
NP_001140177.1:p.Trp1226Ter
|
|
NM_001146706.1:c.3414G>A
|
NP_001140178.1:p.Trp1138Ter
|
|
NM_004653.4:c.3585G>A
|
NP_004644.2:p.Trp1195Ter
|
|
XM_005262560.1:c.3450G>A
|
XP_005262617.1:p.Trp1150Ter
|
|
XM_005262561.1:c.3354G>A
|
XP_005262618.1:p.Trp1118Ter
|
|
XM_011531468.1:c.3507G>A
|
XP_011529770.1:p.Trp1169Ter
|
|
XR_244571.2:n.3873G>A
|
|
|
XR_430568.2:n.4207G>A
|
|
|
XM_005262560.3:c.3450G>A
|
XP_005262617.1:p.Trp1150Ter
|
|
XM_005262561.3:c.3354G>A
|
XP_005262618.1:p.Trp1118Ter
|
|
XM_011531468.3:c.3507G>A
|
XP_011529770.1:p.Trp1169Ter
|
|
XM_024452495.1:c.1575G>A
|
XP_024308263.1:p.Trp525Ter
|
|
XM_024452496.1:c.1341G>A
|
XP_024308264.1:p.Trp447Ter
|
|
XR_001756009.2:n.4323G>A
|
|
|
XR_001756010.2:n.4323G>A
|
|
|
XR_001756011.2:n.4188G>A
|
|
|
XR_001756012.2:n.4336G>A
|
|
|
XR_001756013.2:n.3654G>A
|
|
|
XR_002958832.1:n.3755G>A
|
|
|
XR_002958834.1:n.3979G>A
|
|
|
XR_002958835.1:n.3862G>A
|
|
|
XR_002958836.1:n.4545G>A
|
|
|
XR_002958837.1:n.4352G>A
|
|
|
XR_244571.4:n.3872G>A
|
|
|
XR_430568.4:n.4206G>A
|
|
|
NM_001146706.2:c.3414G>A
|
NP_001140178.1:p.Trp1138Ter
|
|
NM_004653.5:c.3585G>A
MANE Select
|
NP_004644.2:p.Trp1195Ter
|
|
NM_001146705.2:c.3678G>A
|
NP_001140177.1:p.Trp1226Ter
|
|