ENST00000597188.6:c.804G>T
MANE Select
|
ENSP00000471851.1:p.Met268Ile
|
|
ENST00000270328.8:c.804G>T
|
ENSP00000270328.4:p.Met268Ile
|
|
ENST00000593913.5:c.804G>T
|
ENSP00000469901.1:p.Met268Ile
|
|
ENST00000596466.2:n.753G>T
|
|
|
ENST00000596709.5:n.888G>T
|
|
|
ENST00000596851.5:c.804G>T
|
ENSP00000469559.1:p.Met268Ile
|
|
ENST00000597188.5:c.804G>T
|
ENSP00000471851.1:p.Met268Ile
|
|
NM_030957.3:c.804G>T
|
NP_112219.3:p.Met268Ile
|
|
XM_006722917.2:c.-306G>T
|
XP_006722980.1:n.-306G>T
|
|
XM_011528331.1:c.804G>T
|
XP_011526633.1:p.Met268Ile
|
|
XM_011528332.1:c.804G>T
|
XP_011526634.1:p.Met268Ile
|
|
XM_011528333.1:c.804G>T
|
XP_011526635.1:p.Met268Ile
|
|
XM_011528334.1:c.804G>T
|
XP_011526636.1:p.Met268Ile
|
|
XR_430156.2:n.1080G>T
|
|
|
XR_936208.1:n.1080G>T
|
|
|
XR_936209.1:n.1080G>T
|
|
|
XM_006722917.3:c.-306G>T
|
XP_006722980.1:n.-306G>T
|
|
XM_017027338.2:c.804G>T
|
XP_016882827.1:p.Met268Ile
|
|
XR_001753770.1:n.1640G>T
|
|
|
NM_030957.4:c.804G>T
MANE Select
|
NP_112219.3:p.Met268Ile
|
|