ENST00000697291.1:c.*2390G>T
|
ENSP00000513228.1:n.*2390G>T
|
|
ENST00000648433.1:c.2676G>T
|
ENSP00000496816.1:p.Met892Ile
|
|
ENST00000649426.1:n.37G>T
|
|
|
ENST00000649554.1:n.2403G>T
|
|
|
ENST00000649979.2:c.2793G>T
MANE Select
|
ENSP00000497271.1:p.Met931Ile
|
|
ENST00000679938.1:c.2481G>T
|
ENSP00000505518.1:p.Met827Ile
|
|
ENST00000263642.2:c.2793G>T
|
ENSP00000263642.2:p.Met931Ile
|
|
NM_022168.3:c.2793G>T
|
NP_071451.2:p.Met931Ile
|
|
XM_011511628.1:c.2076G>T
|
XP_011509930.1:p.Met692Ile
|
|
NM_022168.4:c.2793G>T
MANE Select
|
NP_071451.2:p.Met931Ile
|
|