ENST00000649046.1:c.12267T>C
MANE Select
|
ENSP00000496870.1:p.Tyr4089=
|
|
ENST00000649153.1:c.3167T>C
|
|
|
ENST00000650252.1:c.1295T>C
|
ENSP00000496887.1:p.Met432Thr
|
|
ENST00000263816.7:c.12267T>C
|
ENSP00000263816.3:p.Tyr4089=
|
|
NM_004525.2:c.12267T>C
|
NP_004516.2:p.Tyr4089=
|
|
XM_011511183.1:c.12138T>C
|
XP_011509485.1:p.Tyr4046=
|
|
XM_011511184.1:c.9978T>C
|
XP_011509486.1:p.Tyr3326=
|
|
NM_004525.3:c.12267T>C
MANE Select
|
NP_004516.2:p.Tyr4089=
|
|
XM_011511183.3:c.12138T>C
|
XP_011509485.1:p.Tyr4046=
|
|
XM_011511184.2:c.9978T>C
|
XP_011509486.1:p.Tyr3326=
|
|