ENST00000695651.1:n.2521G>T
|
|
|
ENST00000695653.1:c.2082G>T
|
ENSP00000512084.1:p.Arg694Ser
|
|
ENST00000695654.1:c.3198G>T
|
ENSP00000512085.1:p.Arg1066Ser
|
|
ENST00000695689.1:c.144G>T
|
ENSP00000512101.1:n.144G>T
|
|
ENST00000695690.1:n.364G>T
|
|
|
ENST00000695691.1:n.364G>T
|
|
|
ENST00000245907.11:c.4173G>T
MANE Select
|
ENSP00000245907.4:p.Arg1391Ser
|
|
ENST00000245907.10:c.4173G>T
|
ENSP00000245907.4:p.Arg1391Ser
|
|
ENST00000596548.1:c.294G>T
|
ENSP00000469744.1:p.Arg98Ser
|
|
ENST00000599899.5:n.1132G>T
|
|
|
ENST00000601008.1:c.242-4271G>T
|
ENSP00000471384.1:n.242-4271G>T
|
|
NM_000064.3:c.4173G>T
|
NP_000055.2:p.Arg1391Ser
|
|
NM_000064.4:c.4173G>T
MANE Select
|
NP_000055.2:p.Arg1391Ser
|
|