ENST00000328300.11:c.4775G>A
MANE Select
|
ENSP00000331902.7:p.Cys1592Tyr
|
|
ENST00000361603.7:c.4757G>A
|
ENSP00000354505.2:p.Cys1586Tyr
|
|
ENST00000510690.2:n.1269G>A
|
|
|
ENST00000644079.1:n.1261G>A
|
|
|
ENST00000328300.10:c.4775G>A
|
ENSP00000331902.6:p.Cys1592Tyr
|
|
ENST00000361603.6:c.4757G>A
|
ENSP00000354505.2:p.Cys1586Tyr
|
|
ENST00000504541.1:c.173G>A
|
ENSP00000424845.1:p.Cys58Tyr
|
|
ENST00000515658.1:c.325-1422G>A
|
|
|
NM_000495.4:c.4757G>A
|
NP_000486.1:p.Cys1586Tyr
|
|
NM_033380.2:c.4775G>A
|
NP_203699.1:p.Cys1592Tyr
|
|
XM_005262070.2:c.4766G>A
|
XP_005262127.1:p.Cys1589Tyr
|
|
XM_006724616.2:c.4775G>A
|
XP_006724679.1:p.Cys1592Tyr
|
|
XM_011530849.1:c.4451G>A
|
XP_011529151.1:p.Cys1484Tyr
|
|
XM_011530851.1:c.2348G>A
|
XP_011529153.1:p.Cys783Tyr
|
|
XM_011530849.2:c.4790G>A
|
XP_011529151.2:p.Cys1597Tyr
|
|
XM_017029259.2:c.4781G>A
|
XP_016884748.1:p.Cys1594Tyr
|
|
XM_017029260.1:c.4772G>A
|
XP_016884749.1:p.Cys1591Tyr
|
|
XM_017029263.2:c.3110G>A
|
XP_016884752.1:p.Cys1037Tyr
|
|
NM_000495.5:c.4757G>A
|
NP_000486.1:p.Cys1586Tyr
|
|
NM_033380.3:c.4775G>A
MANE Select
|
NP_203699.1:p.Cys1592Tyr
|
|