ENST00000682114.1:c.462G>C
|
ENSP00000507245.1:p.Met154Ile
|
|
ENST00000682478.1:n.652G>C
|
|
|
ENST00000683576.1:n.652G>C
|
|
|
ENST00000683627.1:c.462G>C
|
ENSP00000507533.1:p.Met154Ile
|
|
ENST00000684082.1:c.419G>C
|
ENSP00000508266.1:n.419G>C
|
|
ENST00000684633.1:n.434G>C
|
|
|
ENST00000684678.1:c.458G>C
|
ENSP00000507059.1:n.458G>C
|
|
ENST00000369842.9:c.462G>C
MANE Select
|
ENSP00000358857.4:p.Met154Ile
|
|
ENST00000369835.3:c.357G>C
|
ENSP00000358850.3:p.Met119Ile
|
|
ENST00000369842.8:c.462G>C
|
ENSP00000358857.4:p.Met154Ile
|
|
ENST00000428228.5:c.*367G>C
|
ENSP00000401081.1:n.*367G>C
|
|
ENST00000468294.5:n.501G>C
|
|
|
ENST00000471965.1:n.251G>C
|
|
|
ENST00000485261.1:n.731G>C
|
|
|
ENST00000486738.5:n.899G>C
|
|
|
ENST00000492448.1:n.445G>C
|
|
|
NM_000117.2:c.462G>C , LRG_745t1:c.462G>C
|
NP_000108.1:p.Met154Ile
|
|
XM_024452349.1:c.468G>C
|
XP_024308117.1:p.Met156Ile
|
|
NM_000117.3:c.462G>C
MANE Select
|
NP_000108.1:p.Met154Ile
|
|