ENST00000682565.1:c.7657C>T
|
ENSP00000507671.1:p.Leu2553=
|
|
ENST00000682801.1:c.7657C>T
|
ENSP00000507862.1:p.Leu2553=
|
|
ENST00000682859.1:c.7657C>T
|
ENSP00000508222.1:p.Leu2553=
|
|
ENST00000683791.1:c.1049C>T
|
|
|
ENST00000684460.1:c.5109C>T
|
|
|
ENST00000684548.1:c.7657C>T
|
ENSP00000507421.1:p.Leu2553=
|
|
ENST00000684590.1:c.2104C>T
|
ENSP00000507376.1:p.Leu702=
|
|
ENST00000684656.1:c.5109C>T
|
|
|
ENST00000613296.6:c.8038C>T
MANE Select
|
ENSP00000482968.1:p.Leu2680=
|
|
ENST00000651434.1:c.896-29778C>T
|
|
|
ENST00000423048.5:c.2869C>T
|
ENSP00000399833.1:p.Leu957=
|
|
ENST00000484298.5:c.7912C>T
|
ENSP00000478155.1:p.Leu2638=
|
|
ENST00000613296.4:c.8038C>T
|
ENSP00000482968.1:p.Leu2680=
|
|
ENST00000614410.4:c.8038C>T
|
ENSP00000479094.1:p.Leu2680=
|
|
ENST00000620466.4:n.1841C>T
|
|
|
NM_015120.4:c.8041C>T , LRG_741t1:c.8041C>T
|
NP_055935.4:p.Leu2681=
|
|
NM_001378454.1:c.8038C>T
MANE Select
|
NP_001365383.1:p.Leu2680=
|
|