ENST00000228918.9:c.820G>A
MANE Select
|
ENSP00000228918.4:p.Val274Ile
|
|
ENST00000228918.8:c.820G>A
|
ENSP00000228918.4:p.Val274Ile
|
|
ENST00000441074.3:n.1205G>A
|
|
|
ENST00000539925.5:c.763G>A
|
ENSP00000440875.1:p.Val255Ile
|
|
ENST00000541005.1:n.297G>A
|
|
|
ENST00000541102.1:c.391G>A
|
ENSP00000438605.1:p.Val131Ile
|
|
NM_001270987.1:c.763G>A
|
NP_001257916.1:p.Val255Ile
|
|
NM_002342.2:c.820G>A
|
NP_002333.1:p.Val274Ile
|
|
XM_005253688.1:c.712G>A
|
XP_005253745.1:p.Val238Ile
|
|
XM_005253688.2:c.712G>A
|
XP_005253745.1:p.Val238Ile
|
|
NM_002342.3:c.820G>A
MANE Select
|
NP_002333.1:p.Val274Ile
|
|
NM_001270987.2:c.763G>A
|
NP_001257916.1:p.Val255Ile
|
|