ENST00000328300.11:c.4855G>C
MANE Select
|
ENSP00000331902.7:p.Ala1619Pro
|
|
ENST00000361603.7:c.4837G>C
|
ENSP00000354505.2:p.Ala1613Pro
|
|
ENST00000510690.2:n.1349G>C
|
|
|
ENST00000644079.1:n.1686G>C
|
|
|
ENST00000328300.10:c.4855G>C
|
ENSP00000331902.6:p.Ala1619Pro
|
|
ENST00000361603.6:c.4837G>C
|
ENSP00000354505.2:p.Ala1613Pro
|
|
ENST00000504541.1:c.219+379G>C
|
ENSP00000424845.1:n.219+379G>C
|
|
ENST00000515658.1:c.325-997G>C
|
|
|
NM_000495.4:c.4837G>C
|
NP_000486.1:p.Ala1613Pro
|
|
NM_033380.2:c.4855G>C
|
NP_203699.1:p.Ala1619Pro
|
|
XM_005262070.2:c.4846G>C
|
XP_005262127.1:p.Ala1616Pro
|
|
XM_006724616.2:c.4855G>C
|
XP_006724679.1:p.Ala1619Pro
|
|
XM_011530849.1:c.4531G>C
|
XP_011529151.1:p.Ala1511Pro
|
|
XM_011530851.1:c.2428G>C
|
XP_011529153.1:p.Ala810Pro
|
|
XM_011530849.2:c.4870G>C
|
XP_011529151.2:p.Ala1624Pro
|
|
XM_017029259.2:c.4861G>C
|
XP_016884748.1:p.Ala1621Pro
|
|
XM_017029260.1:c.4852G>C
|
XP_016884749.1:p.Ala1618Pro
|
|
XM_017029263.2:c.3190G>C
|
XP_016884752.1:p.Ala1064Pro
|
|
NM_000495.5:c.4837G>C
|
NP_000486.1:p.Ala1613Pro
|
|
NM_033380.3:c.4855G>C
MANE Select
|
NP_203699.1:p.Ala1619Pro
|
|