ENST00000649046.1:c.12283G>T
MANE Select
|
ENSP00000496870.1:p.Asp4095Tyr
|
|
ENST00000649153.1:c.3183G>T
|
|
|
ENST00000650252.1:c.1311G>T
|
ENSP00000496887.1:p.Arg437Ser
|
|
ENST00000263816.7:c.12283G>T
|
ENSP00000263816.3:p.Asp4095Tyr
|
|
NM_004525.2:c.12283G>T
|
NP_004516.2:p.Asp4095Tyr
|
|
XM_011511183.1:c.12154G>T
|
XP_011509485.1:p.Asp4052Tyr
|
|
XM_011511184.1:c.9994G>T
|
XP_011509486.1:p.Asp3332Tyr
|
|
NM_004525.3:c.12283G>T
MANE Select
|
NP_004516.2:p.Asp4095Tyr
|
|
XM_011511183.3:c.12154G>T
|
XP_011509485.1:p.Asp4052Tyr
|
|
XM_011511184.2:c.9994G>T
|
XP_011509486.1:p.Asp3332Tyr
|
|