ENST00000700012.1:c.464C>G
|
ENSP00000514753.1:p.Thr155Ser
|
|
ENST00000700013.1:c.464C>G
|
ENSP00000514754.1:p.Thr155Ser
|
|
ENST00000700114.1:c.386C>G
|
ENSP00000514808.1:p.Thr129Ser
|
|
ENST00000700115.1:c.446C>G
|
ENSP00000514809.1:p.Thr149Ser
|
|
ENST00000700118.1:c.446C>G
|
ENSP00000514810.1:p.Thr149Ser
|
|
ENST00000700119.1:c.*257C>G
|
ENSP00000514811.1:n.*257C>G
|
|
ENST00000700120.1:n.374C>G
|
|
|
ENST00000275034.5:c.446C>G
MANE Select
|
ENSP00000275034.3:p.Thr149Ser
|
|
ENST00000275034.4:c.446C>G
|
ENSP00000275034.3:p.Thr149Ser
|
|
NM_017934.5:c.446C>G
|
NP_060404.3:p.Thr149Ser
|
|
XM_005248729.3:c.446C>G
|
XP_005248786.1:p.Thr149Ser
|
|
XM_011535917.1:c.446C>G
|
XP_011534219.1:p.Thr149Ser
|
|
XM_011535918.1:c.-71C>G
|
XP_011534220.1:n.-71C>G
|
|
XM_011535919.1:c.446C>G
|
XP_011534221.1:p.Thr149Ser
|
|
XR_942499.1:n.672C>G
|
|
|
NM_017934.6:c.446C>G
|
NP_060404.4:p.Thr149Ser
|
|
XM_005248729.5:c.446C>G
|
XP_005248786.1:p.Thr149Ser
|
|
XM_011535918.3:c.-71C>G
|
XP_011534220.1:n.-71C>G
|
|
XM_017010989.2:c.-1284C>G
|
XP_016866478.1:n.-1284C>G
|
|
XM_017010990.2:c.-1284C>G
|
XP_016866479.1:n.-1284C>G
|
|
NM_017934.7:c.446C>G
MANE Select
|
NP_060404.4:p.Thr149Ser
|
|