ENST00000328300.11:c.4973T>C
MANE Select
|
ENSP00000331902.7:p.Val1658Ala
|
|
ENST00000361603.7:c.4955T>C
|
ENSP00000354505.2:p.Val1652Ala
|
|
ENST00000510690.2:n.1467T>C
|
|
|
ENST00000644079.1:n.1804T>C
|
|
|
ENST00000328300.10:c.4973T>C
|
ENSP00000331902.6:p.Val1658Ala
|
|
ENST00000361603.6:c.4955T>C
|
ENSP00000354505.2:p.Val1652Ala
|
|
ENST00000504541.1:c.219+497T>C
|
ENSP00000424845.1:n.219+497T>C
|
|
ENST00000515658.1:c.325-879T>C
|
|
|
NM_000495.4:c.4955T>C
|
NP_000486.1:p.Val1652Ala
|
|
NM_033380.2:c.4973T>C
|
NP_203699.1:p.Val1658Ala
|
|
XM_005262070.2:c.4964T>C
|
XP_005262127.1:p.Val1655Ala
|
|
XM_006724616.2:c.4973T>C
|
XP_006724679.1:p.Val1658Ala
|
|
XM_011530849.1:c.4649T>C
|
XP_011529151.1:p.Val1550Ala
|
|
XM_011530851.1:c.2546T>C
|
XP_011529153.1:p.Val849Ala
|
|
XM_011530849.2:c.4988T>C
|
XP_011529151.2:p.Val1663Ala
|
|
XM_017029259.2:c.4979T>C
|
XP_016884748.1:p.Val1660Ala
|
|
XM_017029260.1:c.4970T>C
|
XP_016884749.1:p.Val1657Ala
|
|
XM_017029263.2:c.3308T>C
|
XP_016884752.1:p.Val1103Ala
|
|
NM_000495.5:c.4955T>C
|
NP_000486.1:p.Val1652Ala
|
|
NM_033380.3:c.4973T>C
MANE Select
|
NP_203699.1:p.Val1658Ala
|
|