|
NM_006662.3:c.9052C>T
MANE Select
|
NP_006653.2:p.Arg3018Trp
|
|
ENST00000262518.9:c.9052C>T
MANE Select
|
ENSP00000262518.4:p.Arg3018Trp
|
|
NM_006662.2:c.9052C>T
|
NP_006653.2:p.Arg3018Trp
|
|
ENST00000262518.8:c.9052C>T
|
ENSP00000262518.4:p.Arg3018Trp
|
|
ENST00000380361.7:c.8521C>T
|
ENSP00000369719.3:p.Arg2841Trp
|
|
ENST00000395059.6:c.8275C>T
|
ENSP00000378499.3:p.Arg2759Trp
|
|
ENST00000411466.7:c.9052C>T
|
ENSP00000405186.3:p.Arg3018Trp
|
|
ENST00000704023.1:c.1758+1137C>T
|
|
|
ENST00000706321.1:c.9052C>T
|
ENSP00000516346.1:p.Arg3018Trp
|