ENST00000317961.9:c.3608T>C
MANE Select
|
ENSP00000322408.4:p.Val1203Ala
|
|
ENST00000317961.8:c.3608T>C
|
ENSP00000322408.4:p.Val1203Ala
|
|
ENST00000382806.6:c.3437T>C
|
ENSP00000372256.2:p.Val1146Ala
|
|
ENST00000415360.1:c.524T>C
|
ENSP00000389433.1:p.Val175Ala
|
|
ENST00000440077.5:c.3485T>C
|
ENSP00000398543.1:p.Val1162Ala
|
|
ENST00000469599.6:n.2206T>C
|
|
|
ENST00000492117.1:n.3500T>C
|
|
|
ENST00000541639.5:c.3701T>C
|
ENSP00000444293.1:p.Val1234Ala
|
|
NM_001146705.1:c.3701T>C
|
NP_001140177.1:p.Val1234Ala
|
|
NM_001146706.1:c.3437T>C
|
NP_001140178.1:p.Val1146Ala
|
|
NM_004653.4:c.3608T>C
|
NP_004644.2:p.Val1203Ala
|
|
XM_005262560.1:c.3473T>C
|
XP_005262617.1:p.Val1158Ala
|
|
XM_005262561.1:c.3377T>C
|
XP_005262618.1:p.Val1126Ala
|
|
XM_011531468.1:c.3530T>C
|
XP_011529770.1:p.Val1177Ala
|
|
XR_244571.2:n.3896T>C
|
|
|
XR_430568.2:n.4230T>C
|
|
|
XM_005262560.3:c.3473T>C
|
XP_005262617.1:p.Val1158Ala
|
|
XM_005262561.3:c.3377T>C
|
XP_005262618.1:p.Val1126Ala
|
|
XM_011531468.3:c.3530T>C
|
XP_011529770.1:p.Val1177Ala
|
|
XM_024452495.1:c.1598T>C
|
XP_024308263.1:p.Val533Ala
|
|
XM_024452496.1:c.1364T>C
|
XP_024308264.1:p.Val455Ala
|
|
XR_001756009.2:n.4346T>C
|
|
|
XR_001756010.2:n.4346T>C
|
|
|
XR_001756011.2:n.4211T>C
|
|
|
XR_001756012.2:n.4359T>C
|
|
|
XR_001756013.2:n.3677T>C
|
|
|
XR_002958832.1:n.3778T>C
|
|
|
XR_002958834.1:n.4002T>C
|
|
|
XR_002958835.1:n.3885T>C
|
|
|
XR_002958836.1:n.4568T>C
|
|
|
XR_002958837.1:n.4375T>C
|
|
|
XR_244571.4:n.3895T>C
|
|
|
XR_430568.4:n.4229T>C
|
|
|
NM_001146706.2:c.3437T>C
|
NP_001140178.1:p.Val1146Ala
|
|
NM_004653.5:c.3608T>C
MANE Select
|
NP_004644.2:p.Val1203Ala
|
|
NM_001146705.2:c.3701T>C
|
NP_001140177.1:p.Val1234Ala
|
|