ENST00000328300.11:c.4327T>C
MANE Select
|
ENSP00000331902.7:p.Leu1443=
|
|
ENST00000361603.7:c.4309T>C
|
ENSP00000354505.2:p.Leu1437=
|
|
ENST00000510690.2:n.821T>C
|
|
|
ENST00000328300.10:c.4327T>C
|
ENSP00000331902.6:p.Leu1443=
|
|
ENST00000361603.6:c.4309T>C
|
ENSP00000354505.2:p.Leu1437=
|
|
ENST00000489230.1:n.730T>C
|
|
|
ENST00000515658.1:c.123T>C
|
|
|
NM_000495.4:c.4309T>C
|
NP_000486.1:p.Leu1437=
|
|
NM_033380.2:c.4327T>C
|
NP_203699.1:p.Leu1443=
|
|
XM_005262070.2:c.4318T>C
|
XP_005262127.1:p.Leu1440=
|
|
XM_006724616.2:c.4327T>C
|
XP_006724679.1:p.Leu1443=
|
|
XM_011530849.1:c.4003T>C
|
XP_011529151.1:p.Leu1335=
|
|
XM_011530851.1:c.1900T>C
|
XP_011529153.1:p.Leu634=
|
|
XM_011530849.2:c.4342T>C
|
XP_011529151.2:p.Leu1448=
|
|
XM_017029259.2:c.4333T>C
|
XP_016884748.1:p.Leu1445=
|
|
XM_017029260.1:c.4324T>C
|
XP_016884749.1:p.Leu1442=
|
|
XM_017029263.2:c.2662T>C
|
XP_016884752.1:p.Leu888=
|
|
NM_000495.5:c.4309T>C
|
NP_000486.1:p.Leu1437=
|
|
NM_033380.3:c.4327T>C
MANE Select
|
NP_203699.1:p.Leu1443=
|
|