ENST00000328300.11:c.4787G>T
MANE Select
|
ENSP00000331902.7:p.Trp1596Leu
|
|
ENST00000361603.7:c.4769G>T
|
ENSP00000354505.2:p.Trp1590Leu
|
|
ENST00000510690.2:n.1281G>T
|
|
|
ENST00000644079.1:n.1273G>T
|
|
|
ENST00000328300.10:c.4787G>T
|
ENSP00000331902.6:p.Trp1596Leu
|
|
ENST00000361603.6:c.4769G>T
|
ENSP00000354505.2:p.Trp1590Leu
|
|
ENST00000504541.1:c.185G>T
|
ENSP00000424845.1:p.Trp62Leu
|
|
ENST00000515658.1:c.325-1410G>T
|
|
|
NM_000495.4:c.4769G>T
|
NP_000486.1:p.Trp1590Leu
|
|
NM_033380.2:c.4787G>T
|
NP_203699.1:p.Trp1596Leu
|
|
XM_005262070.2:c.4778G>T
|
XP_005262127.1:p.Trp1593Leu
|
|
XM_006724616.2:c.4787G>T
|
XP_006724679.1:p.Trp1596Leu
|
|
XM_011530849.1:c.4463G>T
|
XP_011529151.1:p.Trp1488Leu
|
|
XM_011530851.1:c.2360G>T
|
XP_011529153.1:p.Trp787Leu
|
|
XM_011530849.2:c.4802G>T
|
XP_011529151.2:p.Trp1601Leu
|
|
XM_017029259.2:c.4793G>T
|
XP_016884748.1:p.Trp1598Leu
|
|
XM_017029260.1:c.4784G>T
|
XP_016884749.1:p.Trp1595Leu
|
|
XM_017029263.2:c.3122G>T
|
XP_016884752.1:p.Trp1041Leu
|
|
NM_000495.5:c.4769G>T
|
NP_000486.1:p.Trp1590Leu
|
|
NM_033380.3:c.4787G>T
MANE Select
|
NP_203699.1:p.Trp1596Leu
|
|