ENST00000251810.8:c.935T>C
MANE Select
|
ENSP00000251810.3:p.Met312Thr
|
|
ENST00000251810.7:c.935T>C
|
ENSP00000251810.3:p.Met312Thr
|
|
ENST00000395910.6:n.322T>C
|
|
|
ENST00000395912.6:c.779T>C
|
ENSP00000379248.2:p.Met260Thr
|
|
ENST00000519317.5:c.299T>C
|
ENSP00000430641.1:p.Met100Thr
|
|
ENST00000519962.5:c.80T>C
|
ENSP00000429140.1:p.Met27Thr
|
|
ENST00000522368.5:c.1104T>C
|
|
|
ENST00000522394.1:c.268T>C
|
ENSP00000429578.1:n.268T>C
|
|
ENST00000621845.1:c.773T>C
|
ENSP00000484318.1:p.Met258Thr
|
|
NM_001172477.1:c.1151T>C , LRG_788t1:c.1151T>C
|
NP_001165948.1:p.Met384Thr
|
|
NM_001172478.1:c.779T>C
|
NP_001165949.1:p.Met260Thr
|
|
NM_015713.4:c.935T>C , LRG_788t2:c.935T>C
|
NP_056528.2:p.Met312Thr
|
|
NM_001172478.2:c.779T>C
|
NP_001165949.1:p.Met260Thr
|
|
NM_015713.5:c.935T>C
MANE Select
|
NP_056528.2:p.Met312Thr
|
|