ENST00000682565.1:c.7705T>C
|
ENSP00000507671.1:p.Phe2569Leu
|
|
ENST00000682801.1:c.7705T>C
|
ENSP00000507862.1:p.Phe2569Leu
|
|
ENST00000682859.1:c.7705T>C
|
ENSP00000508222.1:p.Phe2569Leu
|
|
ENST00000683791.1:c.1097T>C
|
|
|
ENST00000684460.1:c.5157T>C
|
|
|
ENST00000684548.1:c.7705T>C
|
ENSP00000507421.1:p.Phe2569Leu
|
|
ENST00000684590.1:c.2152T>C
|
ENSP00000507376.1:p.Phe718Leu
|
|
ENST00000684656.1:c.5157T>C
|
|
|
ENST00000613296.6:c.8086T>C
MANE Select
|
ENSP00000482968.1:p.Phe2696Leu
|
|
ENST00000651434.1:c.896-29730T>C
|
|
|
ENST00000423048.5:c.2917T>C
|
ENSP00000399833.1:p.Phe973Leu
|
|
ENST00000484298.5:c.7960T>C
|
ENSP00000478155.1:p.Phe2654Leu
|
|
ENST00000613296.4:c.8086T>C
|
ENSP00000482968.1:p.Phe2696Leu
|
|
ENST00000614410.4:c.8086T>C
|
ENSP00000479094.1:p.Phe2696Leu
|
|
ENST00000620466.4:n.1889T>C
|
|
|
NM_015120.4:c.8089T>C , LRG_741t1:c.8089T>C
|
NP_055935.4:p.Phe2697Leu
|
|
NM_001378454.1:c.8086T>C
MANE Select
|
NP_001365383.1:p.Phe2696Leu
|
|