ENST00000299506.3:c.141G>C
MANE Select
|
ENSP00000299506.3:p.Met47Ile
|
|
ENST00000299506.2:c.141G>C
|
ENSP00000299506.2:p.Met47Ile
|
|
ENST00000305253.8:c.306G>C
|
ENSP00000305426.4:p.Met102Ile
|
|
ENST00000534099.5:c.159G>C
|
ENSP00000434400.1:p.Met53Ile
|
|
NM_003320.4:c.306G>C
|
NP_003311.2:p.Met102Ile
|
|
NM_177972.2:c.141G>C
|
NP_813977.1:p.Met47Ile
|
|
XM_005253109.2:c.267G>C
|
XP_005253166.1:p.Met89Ile
|
|
XM_011520344.1:c.177G>C
|
XP_011518646.1:p.Met59Ile
|
|
XM_005253109.3:c.267G>C
|
XP_005253166.1:p.Met89Ile
|
|
XM_011520344.2:c.177G>C
|
XP_011518646.1:p.Met59Ile
|
|
NM_177972.3:c.141G>C
MANE Select
|
NP_813977.1:p.Met47Ile
|
|
NM_003320.5:c.306G>C
|
NP_003311.2:p.Met102Ile
|
|