ENST00000328300.11:c.5060G>C
MANE Select
|
ENSP00000331902.7:p.Cys1687Ser
|
|
ENST00000361603.7:c.5042G>C
|
ENSP00000354505.2:p.Cys1681Ser
|
|
ENST00000510690.2:n.1554G>C
|
|
|
ENST00000644079.1:n.2748G>C
|
|
|
ENST00000328300.10:c.5060G>C
|
ENSP00000331902.6:p.Cys1687Ser
|
|
ENST00000361603.6:c.5042G>C
|
ENSP00000354505.2:p.Cys1681Ser
|
|
ENST00000504541.1:c.285G>C
|
ENSP00000424845.1:n.285G>C
|
|
ENST00000515658.1:c.390G>C
|
|
|
NM_000495.4:c.5042G>C
|
NP_000486.1:p.Cys1681Ser
|
|
NM_033380.2:c.5060G>C
|
NP_203699.1:p.Cys1687Ser
|
|
XM_005262070.2:c.5051G>C
|
XP_005262127.1:p.Cys1684Ser
|
|
XM_006724616.2:c.5060G>C
|
XP_006724679.1:p.Cys1687Ser
|
|
XM_011530849.1:c.4736G>C
|
XP_011529151.1:p.Cys1579Ser
|
|
XM_011530851.1:c.2633G>C
|
XP_011529153.1:p.Cys878Ser
|
|
XM_011530849.2:c.5075G>C
|
XP_011529151.2:p.Cys1692Ser
|
|
XM_017029259.2:c.5066G>C
|
XP_016884748.1:p.Cys1689Ser
|
|
XM_017029260.1:c.5057G>C
|
XP_016884749.1:p.Cys1686Ser
|
|
XM_017029263.2:c.3395G>C
|
XP_016884752.1:p.Cys1132Ser
|
|
NM_000495.5:c.5042G>C
|
NP_000486.1:p.Cys1681Ser
|
|
NM_033380.3:c.5060G>C
MANE Select
|
NP_203699.1:p.Cys1687Ser
|
|