ENST00000474532.2:c.1189G>T
|
ENSP00000515553.1:p.Asp397Tyr
|
|
ENST00000703916.1:c.1-5014G>T
|
ENSP00000515550.1:n.1-5014G>T
|
|
ENST00000703917.1:c.-1+2597G>T
|
ENSP00000515551.1:n.-1+2597G>T
|
|
ENST00000703918.1:c.1189G>T
|
ENSP00000515552.1:p.Asp397Tyr
|
|
ENST00000703919.1:c.1189G>T
|
ENSP00000515554.1:p.Asp397Tyr
|
|
ENST00000703920.1:c.1189G>T
|
ENSP00000515555.1:p.Asp397Tyr
|
|
ENST00000012134.7:c.1189G>T
|
ENSP00000012134.2:p.Asp397Tyr
|
|
ENST00000367603.8:c.1189G>T
MANE Select
|
ENSP00000356575.2:p.Asp397Tyr
|
|
ENST00000367604.6:c.1189G>T
|
ENSP00000356576.1:p.Asp397Tyr
|
|
ENST00000012134.6:c.1189G>T
|
ENSP00000012134.2:p.Asp397Tyr
|
|
ENST00000367603.6:c.1189G>T
|
ENSP00000356575.2:p.Asp397Tyr
|
|
ENST00000367604.5:c.1189G>T
|
ENSP00000356576.1:p.Asp397Tyr
|
|
NM_006734.3:c.1189G>T
|
NP_006725.3:p.Asp397Tyr
|
|
XM_017010805.1:c.1189G>T
|
XP_016866294.1:p.Asp397Tyr
|
|
XM_024446416.1:c.1189G>T
|
XP_024302184.1:p.Asp397Tyr
|
|
XM_024446417.1:c.1189G>T
|
XP_024302185.1:p.Asp397Tyr
|
|
XM_024446418.1:c.1189G>T
|
XP_024302186.1:p.Asp397Tyr
|
|
XM_024446419.1:c.1189G>T
|
XP_024302187.1:p.Asp397Tyr
|
|
NM_006734.4:c.1189G>T
MANE Select
|
NP_006725.3:p.Asp397Tyr
|
|