ENST00000317961.9:c.3686T>C
MANE Select
|
ENSP00000322408.4:p.Phe1229Ser
|
|
ENST00000317961.8:c.3686T>C
|
ENSP00000322408.4:p.Phe1229Ser
|
|
ENST00000382806.6:c.3515T>C
|
ENSP00000372256.2:p.Phe1172Ser
|
|
ENST00000415360.1:c.602T>C
|
ENSP00000389433.1:p.Phe201Ser
|
|
ENST00000440077.5:c.3563T>C
|
ENSP00000398543.1:p.Phe1188Ser
|
|
ENST00000469599.6:n.2284T>C
|
|
|
ENST00000492117.1:n.3578T>C
|
|
|
ENST00000541639.5:c.3779T>C
|
ENSP00000444293.1:p.Phe1260Ser
|
|
NM_001146705.1:c.3779T>C
|
NP_001140177.1:p.Phe1260Ser
|
|
NM_001146706.1:c.3515T>C
|
NP_001140178.1:p.Phe1172Ser
|
|
NM_004653.4:c.3686T>C
|
NP_004644.2:p.Phe1229Ser
|
|
XM_005262560.1:c.3551T>C
|
XP_005262617.1:p.Phe1184Ser
|
|
XM_005262561.1:c.3455T>C
|
XP_005262618.1:p.Phe1152Ser
|
|
XM_011531468.1:c.3608T>C
|
XP_011529770.1:p.Phe1203Ser
|
|
XR_244571.2:n.3974T>C
|
|
|
XR_430568.2:n.4308T>C
|
|
|
XM_005262560.3:c.3551T>C
|
XP_005262617.1:p.Phe1184Ser
|
|
XM_005262561.3:c.3455T>C
|
XP_005262618.1:p.Phe1152Ser
|
|
XM_011531468.3:c.3608T>C
|
XP_011529770.1:p.Phe1203Ser
|
|
XM_024452495.1:c.1676T>C
|
XP_024308263.1:p.Phe559Ser
|
|
XM_024452496.1:c.1442T>C
|
XP_024308264.1:p.Phe481Ser
|
|
XR_001756009.2:n.4424T>C
|
|
|
XR_001756010.2:n.4424T>C
|
|
|
XR_001756011.2:n.4289T>C
|
|
|
XR_001756012.2:n.4437T>C
|
|
|
XR_001756013.2:n.3755T>C
|
|
|
XR_002958832.1:n.3856T>C
|
|
|
XR_002958834.1:n.4080T>C
|
|
|
XR_002958835.1:n.3963T>C
|
|
|
XR_002958836.1:n.4646T>C
|
|
|
XR_002958837.1:n.4453T>C
|
|
|
XR_244571.4:n.3973T>C
|
|
|
XR_430568.4:n.4307T>C
|
|
|
NM_001146706.2:c.3515T>C
|
NP_001140178.1:p.Phe1172Ser
|
|
NM_004653.5:c.3686T>C
MANE Select
|
NP_004644.2:p.Phe1229Ser
|
|
NM_001146705.2:c.3779T>C
|
NP_001140177.1:p.Phe1260Ser
|
|