ENST00000496887.7:c.745G>A
|
ENSP00000434560.2:p.Ala249Thr
|
|
ENST00000646564.2:c.562G>A
|
ENSP00000495806.2:p.Ala188Thr
|
|
ENST00000155840.12:c.1006G>A
MANE Select
|
ENSP00000155840.2:p.Ala336Thr
|
|
ENST00000335475.6:c.625G>A
|
ENSP00000334497.5:p.Ala209Thr
|
|
ENST00000646564.1:c.208G>A
|
ENSP00000495806.1:p.Ala70Thr
|
|
ENST00000155840.9:c.1006G>A
|
ENSP00000155840.2:p.Ala336Thr
|
|
ENST00000335475.5:c.625G>A
|
ENSP00000334497.5:p.Ala209Thr
|
|
NM_000218.2:c.1006G>A , LRG_287t1:c.1006G>A
|
NP_000209.2:p.Ala336Thr
|
|
NM_181798.1:c.625G>A , LRG_287t2:c.625G>A
|
NP_861463.1:p.Ala209Thr
|
|
NM_000218.3:c.1006G>A
MANE Select
|
NP_000209.2:p.Ala336Thr
|
|