ENST00000475778.2:n.1057G>T
|
|
|
ENST00000683214.1:n.739G>T
|
|
|
ENST00000684143.1:c.628G>T
|
ENSP00000508264.1:p.Asp210Tyr
|
|
ENST00000684745.1:n.305G>T
|
|
|
ENST00000379374.5:c.631G>T
MANE Select
|
ENSP00000368682.4:p.Asp211Tyr
|
|
ENST00000379374.4:c.631G>T
|
ENSP00000368682.4:p.Asp211Tyr
|
|
NM_000444.5:c.631G>T
|
NP_000435.3:p.Asp211Tyr
|
|
NM_001282754.1:c.631G>T
|
NP_001269683.1:p.Asp211Tyr
|
|
XM_011545535.1:c.631G>T
|
XP_011543837.1:p.Asp211Tyr
|
|
XM_017029579.1:c.-93-12759G>T
|
XP_016885068.1:n.-93-12759G>T
|
|
XM_024452390.1:c.340G>T
|
XP_024308158.1:p.Asp114Tyr
|
|
XR_001755695.1:n.1310G>T
|
|
|
NM_000444.6:c.631G>T
MANE Select
|
NP_000435.3:p.Asp211Tyr
|
|
NM_001282754.2:c.631G>T
|
NP_001269683.1:p.Asp211Tyr
|
|