ENST00000328300.11:c.4905C>G
MANE Select
|
ENSP00000331902.7:p.Phe1635Leu
|
|
ENST00000361603.7:c.4887C>G
|
ENSP00000354505.2:p.Phe1629Leu
|
|
ENST00000510690.2:n.1399C>G
|
|
|
ENST00000644079.1:n.1736C>G
|
|
|
ENST00000328300.10:c.4905C>G
|
ENSP00000331902.6:p.Phe1635Leu
|
|
ENST00000361603.6:c.4887C>G
|
ENSP00000354505.2:p.Phe1629Leu
|
|
ENST00000504541.1:c.219+429C>G
|
ENSP00000424845.1:n.219+429C>G
|
|
ENST00000515658.1:c.325-947C>G
|
|
|
NM_000495.4:c.4887C>G
|
NP_000486.1:p.Phe1629Leu
|
|
NM_033380.2:c.4905C>G
|
NP_203699.1:p.Phe1635Leu
|
|
XM_005262070.2:c.4896C>G
|
XP_005262127.1:p.Phe1632Leu
|
|
XM_006724616.2:c.4905C>G
|
XP_006724679.1:p.Phe1635Leu
|
|
XM_011530849.1:c.4581C>G
|
XP_011529151.1:p.Phe1527Leu
|
|
XM_011530851.1:c.2478C>G
|
XP_011529153.1:p.Phe826Leu
|
|
XM_011530849.2:c.4920C>G
|
XP_011529151.2:p.Phe1640Leu
|
|
XM_017029259.2:c.4911C>G
|
XP_016884748.1:p.Phe1637Leu
|
|
XM_017029260.1:c.4902C>G
|
XP_016884749.1:p.Phe1634Leu
|
|
XM_017029263.2:c.3240C>G
|
XP_016884752.1:p.Phe1080Leu
|
|
NM_000495.5:c.4887C>G
|
NP_000486.1:p.Phe1629Leu
|
|
NM_033380.3:c.4905C>G
MANE Select
|
NP_203699.1:p.Phe1635Leu
|
|