ENST00000317961.9:c.3539T>C
MANE Select
|
ENSP00000322408.4:p.Val1180Ala
|
|
ENST00000317961.8:c.3539T>C
|
ENSP00000322408.4:p.Val1180Ala
|
|
ENST00000382806.6:c.3368T>C
|
ENSP00000372256.2:p.Val1123Ala
|
|
ENST00000415360.1:c.455T>C
|
ENSP00000389433.1:p.Val152Ala
|
|
ENST00000440077.5:c.3416T>C
|
ENSP00000398543.1:p.Val1139Ala
|
|
ENST00000469599.6:n.2137T>C
|
|
|
ENST00000492117.1:n.3431T>C
|
|
|
ENST00000541639.5:c.3632T>C
|
ENSP00000444293.1:p.Val1211Ala
|
|
NM_001146705.1:c.3632T>C
|
NP_001140177.1:p.Val1211Ala
|
|
NM_001146706.1:c.3368T>C
|
NP_001140178.1:p.Val1123Ala
|
|
NM_004653.4:c.3539T>C
|
NP_004644.2:p.Val1180Ala
|
|
XM_005262560.1:c.3404T>C
|
XP_005262617.1:p.Val1135Ala
|
|
XM_005262561.1:c.3308T>C
|
XP_005262618.1:p.Val1103Ala
|
|
XM_011531468.1:c.3461T>C
|
XP_011529770.1:p.Val1154Ala
|
|
XR_244571.2:n.3827T>C
|
|
|
XR_430568.2:n.4161T>C
|
|
|
XM_005262560.3:c.3404T>C
|
XP_005262617.1:p.Val1135Ala
|
|
XM_005262561.3:c.3308T>C
|
XP_005262618.1:p.Val1103Ala
|
|
XM_011531468.3:c.3461T>C
|
XP_011529770.1:p.Val1154Ala
|
|
XM_024452495.1:c.1529T>C
|
XP_024308263.1:p.Val510Ala
|
|
XM_024452496.1:c.1295T>C
|
XP_024308264.1:p.Val432Ala
|
|
XR_001756009.2:n.4277T>C
|
|
|
XR_001756010.2:n.4277T>C
|
|
|
XR_001756011.2:n.4142T>C
|
|
|
XR_001756012.2:n.4290T>C
|
|
|
XR_001756013.2:n.3608T>C
|
|
|
XR_002958832.1:n.3709T>C
|
|
|
XR_002958834.1:n.3933T>C
|
|
|
XR_002958835.1:n.3816T>C
|
|
|
XR_002958836.1:n.4499T>C
|
|
|
XR_002958837.1:n.4306T>C
|
|
|
XR_244571.4:n.3826T>C
|
|
|
XR_430568.4:n.4160T>C
|
|
|
NM_001146706.2:c.3368T>C
|
NP_001140178.1:p.Val1123Ala
|
|
NM_004653.5:c.3539T>C
MANE Select
|
NP_004644.2:p.Val1180Ala
|
|
NM_001146705.2:c.3632T>C
|
NP_001140177.1:p.Val1211Ala
|
|