ENST00000682565.1:c.7751T>C
|
ENSP00000507671.1:p.Phe2584Ser
|
|
ENST00000682801.1:c.7751T>C
|
ENSP00000507862.1:p.Phe2584Ser
|
|
ENST00000682859.1:c.7751T>C
|
ENSP00000508222.1:p.Phe2584Ser
|
|
ENST00000683791.1:c.1143T>C
|
|
|
ENST00000684460.1:c.5203T>C
|
|
|
ENST00000684548.1:c.7751T>C
|
ENSP00000507421.1:p.Phe2584Ser
|
|
ENST00000684590.1:c.2198T>C
|
ENSP00000507376.1:p.Phe733Ser
|
|
ENST00000684656.1:c.5203T>C
|
|
|
ENST00000613296.6:c.8132T>C
MANE Select
|
ENSP00000482968.1:p.Phe2711Ser
|
|
ENST00000651434.1:c.896-29684T>C
|
|
|
ENST00000423048.5:c.2963T>C
|
ENSP00000399833.1:p.Phe988Ser
|
|
ENST00000484298.5:c.8006T>C
|
ENSP00000478155.1:p.Phe2669Ser
|
|
ENST00000613296.4:c.8132T>C
|
ENSP00000482968.1:p.Phe2711Ser
|
|
ENST00000614410.4:c.8132T>C
|
ENSP00000479094.1:p.Phe2711Ser
|
|
ENST00000620466.4:n.1935T>C
|
|
|
NM_015120.4:c.8135T>C , LRG_741t1:c.8135T>C
|
NP_055935.4:p.Phe2712Ser
|
|
NM_001378454.1:c.8132T>C
MANE Select
|
NP_001365383.1:p.Phe2711Ser
|
|