ENST00000317961.9:c.3394T>G
MANE Select
|
ENSP00000322408.4:p.Ser1132Ala
|
|
ENST00000317961.8:c.3394T>G
|
ENSP00000322408.4:p.Ser1132Ala
|
|
ENST00000382806.6:c.3223T>G
|
ENSP00000372256.2:p.Ser1075Ala
|
|
ENST00000415360.1:c.310T>G
|
ENSP00000389433.1:p.Ser104Ala
|
|
ENST00000440077.5:c.3271T>G
|
ENSP00000398543.1:p.Ser1091Ala
|
|
ENST00000469599.6:n.1992T>G
|
|
|
ENST00000492117.1:n.3286T>G
|
|
|
ENST00000541639.5:c.3487T>G
|
ENSP00000444293.1:p.Ser1163Ala
|
|
NM_001146705.1:c.3487T>G
|
NP_001140177.1:p.Ser1163Ala
|
|
NM_001146706.1:c.3223T>G
|
NP_001140178.1:p.Ser1075Ala
|
|
NM_004653.4:c.3394T>G
|
NP_004644.2:p.Ser1132Ala
|
|
XM_005262560.1:c.3259T>G
|
XP_005262617.1:p.Ser1087Ala
|
|
XM_005262561.1:c.3163T>G
|
XP_005262618.1:p.Ser1055Ala
|
|
XM_011531468.1:c.3316T>G
|
XP_011529770.1:p.Ser1106Ala
|
|
XR_244571.2:n.3682T>G
|
|
|
XR_430568.2:n.4016T>G
|
|
|
XM_005262560.3:c.3259T>G
|
XP_005262617.1:p.Ser1087Ala
|
|
XM_005262561.3:c.3163T>G
|
XP_005262618.1:p.Ser1055Ala
|
|
XM_011531468.3:c.3316T>G
|
XP_011529770.1:p.Ser1106Ala
|
|
XM_024452495.1:c.1384T>G
|
XP_024308263.1:p.Ser462Ala
|
|
XM_024452496.1:c.1150T>G
|
XP_024308264.1:p.Ser384Ala
|
|
XR_001756009.2:n.4132T>G
|
|
|
XR_001756010.2:n.4132T>G
|
|
|
XR_001756011.2:n.3997T>G
|
|
|
XR_001756012.2:n.4145T>G
|
|
|
XR_001756013.2:n.3463T>G
|
|
|
XR_002958832.1:n.3564T>G
|
|
|
XR_002958834.1:n.3788T>G
|
|
|
XR_002958835.1:n.3671T>G
|
|
|
XR_002958836.1:n.4354T>G
|
|
|
XR_002958837.1:n.4161T>G
|
|
|
XR_244571.4:n.3681T>G
|
|
|
XR_430568.4:n.4015T>G
|
|
|
NM_001146706.2:c.3223T>G
|
NP_001140178.1:p.Ser1075Ala
|
|
NM_004653.5:c.3394T>G
MANE Select
|
NP_004644.2:p.Ser1132Ala
|
|
NM_001146705.2:c.3487T>G
|
NP_001140177.1:p.Ser1163Ala
|
|