ENST00000328300.11:c.5030T>G
MANE Select
|
ENSP00000331902.7:p.Leu1677Trp
|
|
ENST00000361603.7:c.5012T>G
|
ENSP00000354505.2:p.Leu1671Trp
|
|
ENST00000510690.2:n.1524T>G
|
|
|
ENST00000644079.1:n.2718T>G
|
|
|
ENST00000328300.10:c.5030T>G
|
ENSP00000331902.6:p.Leu1677Trp
|
|
ENST00000361603.6:c.5012T>G
|
ENSP00000354505.2:p.Leu1671Trp
|
|
ENST00000504541.1:c.255T>G
|
ENSP00000424845.1:n.255T>G
|
|
ENST00000515658.1:c.360T>G
|
|
|
NM_000495.4:c.5012T>G
|
NP_000486.1:p.Leu1671Trp
|
|
NM_033380.2:c.5030T>G
|
NP_203699.1:p.Leu1677Trp
|
|
XM_005262070.2:c.5021T>G
|
XP_005262127.1:p.Leu1674Trp
|
|
XM_006724616.2:c.5030T>G
|
XP_006724679.1:p.Leu1677Trp
|
|
XM_011530849.1:c.4706T>G
|
XP_011529151.1:p.Leu1569Trp
|
|
XM_011530851.1:c.2603T>G
|
XP_011529153.1:p.Leu868Trp
|
|
XM_011530849.2:c.5045T>G
|
XP_011529151.2:p.Leu1682Trp
|
|
XM_017029259.2:c.5036T>G
|
XP_016884748.1:p.Leu1679Trp
|
|
XM_017029260.1:c.5027T>G
|
XP_016884749.1:p.Leu1676Trp
|
|
XM_017029263.2:c.3365T>G
|
XP_016884752.1:p.Leu1122Trp
|
|
NM_000495.5:c.5012T>G
|
NP_000486.1:p.Leu1671Trp
|
|
NM_033380.3:c.5030T>G
MANE Select
|
NP_203699.1:p.Leu1677Trp
|
|