ENST00000299084.9:c.1106T>G
MANE Select
|
ENSP00000299084.4:p.Met369Arg
|
|
ENST00000299084.8:c.1106T>G
|
ENSP00000299084.4:p.Met369Arg
|
|
NM_152594.2:c.1106T>G
|
NP_689807.1:p.Met369Arg
|
|
XM_005254202.2:c.1142T>G
|
XP_005254259.1:p.Met381Arg
|
|
XM_005254203.3:c.884T>G
|
XP_005254260.1:p.Met295Arg
|
|
XM_011521288.1:c.1043T>G
|
XP_011519590.1:p.Met348Arg
|
|
XM_011521289.1:c.1043T>G
|
XP_011519591.1:p.Met348Arg
|
|
XM_011521290.1:c.1043T>G
|
XP_011519592.1:p.Met348Arg
|
|
XM_005254202.3:c.1142T>G
|
XP_005254259.1:p.Met381Arg
|
|
XM_011521289.3:c.1043T>G
|
XP_011519591.1:p.Met348Arg
|
|
NM_152594.3:c.1106T>G
MANE Select
|
NP_689807.1:p.Met369Arg
|
|