ENST00000328300.11:c.4494A>C
MANE Select
|
ENSP00000331902.7:p.Val1498=
|
|
ENST00000361603.7:c.4476A>C
|
ENSP00000354505.2:p.Val1492=
|
|
ENST00000510690.2:n.988A>C
|
|
|
ENST00000328300.10:c.4494A>C
|
ENSP00000331902.6:p.Val1498=
|
|
ENST00000361603.6:c.4476A>C
|
ENSP00000354505.2:p.Val1492=
|
|
ENST00000515658.1:c.290A>C
|
|
|
NM_000495.4:c.4476A>C
|
NP_000486.1:p.Val1492=
|
|
NM_033380.2:c.4494A>C
|
NP_203699.1:p.Val1498=
|
|
XM_005262070.2:c.4485A>C
|
XP_005262127.1:p.Val1495=
|
|
XM_006724616.2:c.4494A>C
|
XP_006724679.1:p.Val1498=
|
|
XM_011530849.1:c.4170A>C
|
XP_011529151.1:p.Val1390=
|
|
XM_011530851.1:c.2067A>C
|
XP_011529153.1:p.Val689=
|
|
XM_011530849.2:c.4509A>C
|
XP_011529151.2:p.Val1503=
|
|
XM_017029259.2:c.4500A>C
|
XP_016884748.1:p.Val1500=
|
|
XM_017029260.1:c.4491A>C
|
XP_016884749.1:p.Val1497=
|
|
XM_017029263.2:c.2829A>C
|
XP_016884752.1:p.Val943=
|
|
NM_000495.5:c.4476A>C
|
NP_000486.1:p.Val1492=
|
|
NM_033380.3:c.4494A>C
MANE Select
|
NP_203699.1:p.Val1498=
|
|