ENST00000411466.7:c.8242C>T
|
ENSP00000405186.3:p.Arg2748Ter
|
|
ENST00000704023.1:c.1758+327C>T
|
|
|
ENST00000706321.1:c.8242C>T
|
ENSP00000516346.1:p.Arg2748Ter
|
|
ENST00000262518.9:c.8242C>T
MANE Select
|
ENSP00000262518.4:p.Arg2748Ter
|
|
ENST00000262518.8:c.8242C>T
|
ENSP00000262518.4:p.Arg2748Ter
|
|
ENST00000380361.7:c.7711C>T
|
ENSP00000369719.3:p.Arg2571Ter
|
|
ENST00000395059.6:c.7465C>T
|
ENSP00000378499.3:p.Arg2489Ter
|
|
NM_006662.2:c.8242C>T
|
NP_006653.2:p.Arg2748Ter
|
|
NM_006662.3:c.8242C>T
MANE Select
|
NP_006653.2:p.Arg2748Ter
|
|