ENST00000545399.6:c.1836A>T
|
ENSP00000444688.1:p.Ala612=
|
|
ENST00000644613.1:c.1797A>T
|
ENSP00000494711.1:p.Ala599=
|
|
ENST00000648268.1:c.1797A>T
MANE Select
|
ENSP00000498113.1:p.Ala599=
|
|
ENST00000302102.9:c.1797A>T
|
ENSP00000302397.5:p.Ala599=
|
|
ENST00000441343.5:c.1797A>T
|
ENSP00000411503.1:p.Ala599=
|
|
ENST00000543770.5:c.1830A>T
|
ENSP00000437577.1:p.Ala610=
|
|
ENST00000545399.5:c.1836A>T
|
ENSP00000444688.1:p.Ala612=
|
|
ENST00000602133.5:c.1707A>T
|
ENSP00000471581.1:p.Ala569=
|
|
NM_001256213.1:c.1830A>T
|
NP_001243142.1:p.Ala610=
|
|
NM_001256214.1:c.1836A>T
|
NP_001243143.1:p.Ala612=
|
|
NM_152296.4:c.1797A>T
|
NP_689509.1:p.Ala599=
|
|
XM_011526991.1:c.1707A>T
|
XP_011525293.1:p.Ala569=
|
|
NM_152296.5:c.1797A>T
MANE Select
|
NP_689509.1:p.Ala599=
|
|
NM_001256214.2:c.1836A>T
|
NP_001243143.1:p.Ala612=
|
|
NM_001256213.2:c.1830A>T
|
NP_001243142.1:p.Ala610=
|
|