ENST00000328300.11:c.4631G>A
MANE Select
|
ENSP00000331902.7:p.Trp1544Ter
|
|
ENST00000361603.7:c.4613G>A
|
ENSP00000354505.2:p.Trp1538Ter
|
|
ENST00000510690.2:n.1125G>A
|
|
|
ENST00000328300.10:c.4631G>A
|
ENSP00000331902.6:p.Trp1544Ter
|
|
ENST00000361603.6:c.4613G>A
|
ENSP00000354505.2:p.Trp1538Ter
|
|
ENST00000504541.1:c.29G>A
|
ENSP00000424845.1:p.Trp10Ter
|
|
ENST00000515658.1:c.325-3447G>A
|
|
|
NM_000495.4:c.4613G>A
|
NP_000486.1:p.Trp1538Ter
|
|
NM_033380.2:c.4631G>A
|
NP_203699.1:p.Trp1544Ter
|
|
XM_005262070.2:c.4622G>A
|
XP_005262127.1:p.Trp1541Ter
|
|
XM_006724616.2:c.4631G>A
|
XP_006724679.1:p.Trp1544Ter
|
|
XM_011530849.1:c.4307G>A
|
XP_011529151.1:p.Trp1436Ter
|
|
XM_011530851.1:c.2204G>A
|
XP_011529153.1:p.Trp735Ter
|
|
XM_011530849.2:c.4646G>A
|
XP_011529151.2:p.Trp1549Ter
|
|
XM_017029259.2:c.4637G>A
|
XP_016884748.1:p.Trp1546Ter
|
|
XM_017029260.1:c.4628G>A
|
XP_016884749.1:p.Trp1543Ter
|
|
XM_017029263.2:c.2966G>A
|
XP_016884752.1:p.Trp989Ter
|
|
NM_000495.5:c.4613G>A
|
NP_000486.1:p.Trp1538Ter
|
|
NM_033380.3:c.4631G>A
MANE Select
|
NP_203699.1:p.Trp1544Ter
|
|