ENST00000334268.9:c.1052-9660C>T
MANE Select
|
ENSP00000333984.5:n.1052-9660C>T
|
|
ENST00000662930.1:c.1055-9660C>T
|
ENSP00000499585.1:n.1055-9660C>T
|
|
ENST00000334268.8:c.1052-9660C>T
|
ENSP00000333984.5:n.1052-9660C>T
|
|
NM_001251987.1:c.1055-9660C>T
|
NP_001238916.1:n.1055-9660C>T
|
|
NM_006073.3:c.1052-9660C>T
|
NP_006064.2:n.1052-9660C>T
|
|
XM_011535382.1:c.1052-9660C>T
|
XP_011533684.1:n.1052-9660C>T
|
|
NM_006073.4:c.1052-9660C>T
MANE Select
|
NP_006064.2:n.1052-9660C>T
|
|
NM_001251987.2:c.1055-9660C>T
|
NP_001238916.1:n.1055-9660C>T
|
|