ENST00000622290.5:c.3716A>C
|
ENSP00000483331.2:p.Tyr1239Ser
|
|
ENST00000205557.12:c.3716A>C
MANE Select
|
ENSP00000205557.7:p.Tyr1239Ser
|
|
ENST00000640696.1:c.530A>C
|
ENSP00000492197.1:p.Tyr177Ser
|
|
ENST00000205557.11:c.3716A>C
|
ENSP00000205557.7:p.Tyr1239Ser
|
|
ENST00000456970.6:c.3341A>C
|
ENSP00000405002.2:n.3341A>C
|
|
ENST00000622290.4:c.*925A>C
|
ENSP00000483331.1:n.*925A>C
|
|
NM_001171.5:c.3716A>C
|
NP_001162.4:p.Tyr1239Ser
|
|
XM_011522479.1:c.3683A>C
|
XP_011520781.1:p.Tyr1228Ser
|
|
XM_011522480.1:c.3374A>C
|
XP_011520782.1:p.Tyr1125Ser
|
|
XM_011522481.1:c.3374A>C
|
XP_011520783.1:p.Tyr1125Ser
|
|
XR_932836.1:n.3951A>C
|
|
|
XR_932837.1:n.3752A>C
|
|
|
XR_932838.1:n.3752A>C
|
|
|
XR_933134.1:n.539-280T>G
|
|
|
NM_001351800.1:c.3374A>C
|
NP_001338729.1:p.Tyr1125Ser
|
|
NR_147784.1:n.3378A>C
|
|
|
XM_011522479.2:c.3683A>C
|
XP_011520781.1:p.Tyr1228Ser
|
|
XM_011522481.3:c.3374A>C
|
XP_011520783.1:p.Tyr1125Ser
|
|
XM_017023212.1:c.3548A>C
|
XP_016878701.1:p.Tyr1183Ser
|
|
XM_024450261.1:c.3752A>C
|
XP_024306029.1:p.Tyr1251Ser
|
|
XR_932836.2:n.3897A>C
|
|
|
XR_932837.3:n.3697A>C
|
|
|
XR_932838.3:n.3697A>C
|
|
|
NM_001171.6:c.3716A>C
MANE Select
|
NP_001162.5:p.Tyr1239Ser
|
|