ENST00000394975.3:c.337T>C
MANE Select
|
ENSP00000378426.2:p.Ser113Pro
|
|
ENST00000300851.10:c.398T>C
|
ENSP00000300851.6:p.Val133Ala
|
|
ENST00000319788.11:c.419T>C
|
ENSP00000326135.7:p.Val140Ala
|
|
ENST00000354895.4:c.227T>C
|
ENSP00000346969.4:p.Val76Ala
|
|
ENST00000394971.7:c.431T>C
|
ENSP00000378422.3:p.Val144Ala
|
|
ENST00000394975.2:c.337T>C
|
ENSP00000378426.2:p.Ser113Pro
|
|
ENST00000420057.2:c.299T>C
|
|
|
ENST00000472468.1:c.22T>C
|
ENSP00000458994.1:p.Ser8Pro
|
|
ENST00000498155.1:c.434T>C
|
ENSP00000417662.1:p.Val145Ala
|
|
ENST00000529564.1:c.283+2023T>C
|
ENSP00000431371.1:n.283+2023T>C
|
|
ENST00000532364.1:c.173+3268T>C
|
ENSP00000460316.1:n.173+3268T>C
|
|
ENST00000533518.5:c.210T>C
|
|
|
NM_001311311.1:c.421T>C
|
NP_001298240.1:p.Ser141Pro
|
|
NM_024006.4:c.337T>C
|
NP_076869.1:p.Ser113Pro
|
|
NM_024006.5:c.337T>C
|
NP_076869.1:p.Ser113Pro
|
|
NM_206824.1:c.227T>C
|
NP_996560.1:p.Val76Ala
|
|
NM_206824.2:c.227T>C
|
NP_996560.1:p.Val76Ala
|
|
XM_011545944.1:c.337T>C
|
XP_011544246.1:p.Ser113Pro
|
|
XM_011545945.1:c.227T>C
|
XP_011544247.1:p.Val76Ala
|
|
XR_950848.1:n.1125T>C
|
|
|
NM_024006.6:c.337T>C
MANE Select
|
NP_076869.1:p.Ser113Pro
|
|
NM_001311311.2:c.421T>C
|
NP_001298240.1:p.Ser141Pro
|
|
NM_206824.3:c.227T>C
|
NP_996560.1:p.Val76Ala
|
|