ENST00000649046.1:c.12294C>T
MANE Select
|
ENSP00000496870.1:p.Leu4098=
|
|
ENST00000649153.1:c.3194C>T
|
|
|
ENST00000650252.1:c.1322C>T
|
ENSP00000496887.1:n.1322C>T
|
|
ENST00000263816.7:c.12294C>T
|
ENSP00000263816.3:p.Leu4098=
|
|
NM_004525.2:c.12294C>T
|
NP_004516.2:p.Leu4098=
|
|
XM_011511183.1:c.12165C>T
|
XP_011509485.1:p.Leu4055=
|
|
XM_011511184.1:c.10005C>T
|
XP_011509486.1:p.Leu3335=
|
|
NM_004525.3:c.12294C>T
MANE Select
|
NP_004516.2:p.Leu4098=
|
|
XM_011511183.3:c.12165C>T
|
XP_011509485.1:p.Leu4055=
|
|
XM_011511184.2:c.10005C>T
|
XP_011509486.1:p.Leu3335=
|
|