ENST00000399503.4:c.3085T>G
MANE Select
|
ENSP00000382423.3:p.Phe1029Val
|
|
ENST00000399503.3:c.3085T>G
|
ENSP00000382423.3:p.Phe1029Val
|
|
NM_005921.1:c.3085T>G
|
NP_005912.1:p.Phe1029Val
|
|
XM_005248519.3:c.2707T>G
|
XP_005248576.2:p.Phe903Val
|
|
XM_011543406.1:c.2830T>G
|
XP_011541708.1:p.Phe944Val
|
|
XM_011543407.1:c.2806T>G
|
XP_011541709.1:p.Phe936Val
|
|
XM_011543408.1:c.3085T>G
|
XP_011541710.1:p.Phe1029Val
|
|
XM_017009484.1:c.2674T>G
|
XP_016864973.1:p.Phe892Val
|
|
XM_017009485.1:c.2596T>G
|
XP_016864974.1:p.Phe866Val
|
|
XR_001742068.2:n.3116T>G
|
|
|
NM_005921.2:c.3085T>G
MANE Select
|
NP_005912.1:p.Phe1029Val
|
|