|
ENST00000303354.11:c.647T>C
|
ENSP00000304748.7:p.Phe216Ser
|
|
|
ENST00000409435.6:c.597-157T>C
|
ENSP00000386330.2:n.597-157T>C
|
|
|
ENST00000452182.2:c.647T>C
|
ENSP00000393141.2:p.Phe216Ser
|
|
|
ENST00000454569.6:c.647T>C
|
ENSP00000413212.2:p.Phe216Ser
|
|
|
ENST00000472119.2:n.1002T>C
|
|
|
|
ENST00000642356.2:c.647T>C
MANE Select
|
ENSP00000495601.1:p.Phe216Ser
|
|
|
ENST00000644316.1:c.597-157T>C
|
ENSP00000493939.1:n.597-157T>C
|
|
|
ENST00000645907.1:c.597-157T>C
|
ENSP00000495983.1:n.597-157T>C
|
|
|
ENST00000303354.10:c.647T>C
|
ENSP00000304748.7:p.Phe216Ser
|
|
|
ENST00000409435.5:c.647T>C
|
ENSP00000386330.1:p.Phe216Ser
|
|
|
ENST00000409672.5:c.647T>C
|
ENSP00000386306.1:p.Phe216Ser
|
|
|
ENST00000452182.1:c.192-157T>C
|
ENSP00000393141.1:n.192-157T>C
|
|
|
ENST00000454569.5:c.192-157T>C
|
ENSP00000413212.1:n.192-157T>C
|
|
|
ENST00000472119.1:n.180T>C
|
|
|
|
NM_002977.3:c.647T>C , LRG_369t1:c.647T>C
|
NP_002968.1:p.Phe216Ser
|
|
|
XM_005246757.1:c.647T>C
|
XP_005246814.1:p.Phe216Ser
|
|
|
XM_011511616.1:c.647T>C
|
XP_011509918.1:p.Phe216Ser
|
|
|
XM_011511617.1:c.597-157T>C
|
XP_011509919.1:n.597-157T>C
|
|
|
XM_011511618.1:c.597-157T>C
|
XP_011509920.1:n.597-157T>C
|
|
|
XM_011511619.1:c.647T>C
|
XP_011509921.1:p.Phe216Ser
|
|
|
NM_001365536.1:c.647T>C
MANE Select
|
NP_001352465.1:p.Phe216Ser
|
|
|
XM_011511616.3:c.647T>C
|
XP_011509918.1:p.Phe216Ser
|
|
|
XM_011511617.2:c.597-157T>C
|
XP_011509919.1:n.597-157T>C
|
|
|
XM_011511618.2:c.597-157T>C
|
XP_011509920.1:n.597-157T>C
|
|
|
XM_011511619.2:c.647T>C
|
XP_011509921.1:p.Phe216Ser
|
|
|
XM_017004668.1:c.260T>C
|
XP_016860157.1:p.Phe87Ser
|
|
|
XM_017004669.1:c.-56-977T>C
|
XP_016860158.1:n.-56-977T>C
|
|
|
XR_001738886.1:n.961T>C
|
|
|
