|
ENST00000328300.11:c.4774T>C
MANE Select
|
ENSP00000331902.7:p.Cys1592Arg
|
|
|
ENST00000361603.7:c.4756T>C
|
ENSP00000354505.2:p.Cys1586Arg
|
|
|
ENST00000510690.2:n.1268T>C
|
|
|
|
ENST00000644079.1:n.1260T>C
|
|
|
|
ENST00000328300.10:c.4774T>C
|
ENSP00000331902.6:p.Cys1592Arg
|
|
|
ENST00000361603.6:c.4756T>C
|
ENSP00000354505.2:p.Cys1586Arg
|
|
|
ENST00000504541.1:c.172T>C
|
ENSP00000424845.1:p.Cys58Arg
|
|
|
ENST00000515658.1:c.325-1423T>C
|
|
|
|
NM_000495.4:c.4756T>C
|
NP_000486.1:p.Cys1586Arg
|
|
|
NM_033380.2:c.4774T>C
|
NP_203699.1:p.Cys1592Arg
|
|
|
XM_005262070.2:c.4765T>C
|
XP_005262127.1:p.Cys1589Arg
|
|
|
XM_006724616.2:c.4774T>C
|
XP_006724679.1:p.Cys1592Arg
|
|
|
XM_011530849.1:c.4450T>C
|
XP_011529151.1:p.Cys1484Arg
|
|
|
XM_011530851.1:c.2347T>C
|
XP_011529153.1:p.Cys783Arg
|
|
|
XM_011530849.2:c.4789T>C
|
XP_011529151.2:p.Cys1597Arg
|
|
|
XM_017029259.2:c.4780T>C
|
XP_016884748.1:p.Cys1594Arg
|
|
|
XM_017029260.1:c.4771T>C
|
XP_016884749.1:p.Cys1591Arg
|
|
|
XM_017029263.2:c.3109T>C
|
XP_016884752.1:p.Cys1037Arg
|
|
|
NM_000495.5:c.4756T>C
|
NP_000486.1:p.Cys1586Arg
|
|
|
NM_033380.3:c.4774T>C
MANE Select
|
NP_203699.1:p.Cys1592Arg
|
|
