ENST00000695651.1:n.2692G>T
|
|
|
ENST00000695653.1:c.2253G>T
|
ENSP00000512084.1:p.Leu751=
|
|
ENST00000695654.1:c.3369G>T
|
ENSP00000512085.1:p.Leu1123=
|
|
ENST00000695689.1:c.315G>T
|
ENSP00000512101.1:n.315G>T
|
|
ENST00000695690.1:n.535G>T
|
|
|
ENST00000695691.1:n.535G>T
|
|
|
ENST00000245907.11:c.4344G>T
MANE Select
|
ENSP00000245907.4:p.Leu1448=
|
|
ENST00000245907.10:c.4344G>T
|
ENSP00000245907.4:p.Leu1448=
|
|
ENST00000596548.1:c.465G>T
|
ENSP00000469744.1:p.Leu155=
|
|
ENST00000599899.5:n.1303G>T
|
|
|
ENST00000601008.1:c.242-3989G>T
|
ENSP00000471384.1:n.242-3989G>T
|
|
NM_000064.3:c.4344G>T
|
NP_000055.2:p.Leu1448=
|
|
NM_000064.4:c.4344G>T
MANE Select
|
NP_000055.2:p.Leu1448=
|
|