ENST00000649046.1:c.12186C>A
MANE Select
|
ENSP00000496870.1:p.Val4062=
|
|
ENST00000649153.1:c.3086C>A
|
|
|
ENST00000650252.1:c.1214C>A
|
ENSP00000496887.1:p.Ser405Tyr
|
|
ENST00000263816.7:c.12186C>A
|
ENSP00000263816.3:p.Val4062=
|
|
NM_004525.2:c.12186C>A
|
NP_004516.2:p.Val4062=
|
|
XM_011511183.1:c.12057C>A
|
XP_011509485.1:p.Val4019=
|
|
XM_011511184.1:c.9897C>A
|
XP_011509486.1:p.Val3299=
|
|
NM_004525.3:c.12186C>A
MANE Select
|
NP_004516.2:p.Val4062=
|
|
XM_011511183.3:c.12057C>A
|
XP_011509485.1:p.Val4019=
|
|
XM_011511184.2:c.9897C>A
|
XP_011509486.1:p.Val3299=
|
|