ENST00000247933.9:c.1657C>G
|
ENSP00000247933.4:p.Arg553Gly
|
|
ENST00000514224.2:c.1657C>G
MANE Select
|
ENSP00000425081.2:p.Arg553Gly
|
|
ENST00000652070.1:n.1713C>G
|
|
|
ENST00000247933.8:c.1657C>G
|
ENSP00000247933.4:p.Arg553Gly
|
|
ENST00000514224.1:c.1261C>G
|
ENSP00000425081.1:p.Arg421Gly
|
|
ENST00000514417.1:n.49C>G
|
|
|
ENST00000514698.5:n.1764C>G
|
|
|
NM_000203.4:c.1657C>G
|
NP_000194.2:p.Arg553Gly
|
|
NR_110313.1:n.1745C>G
|
|
|
XM_006713882.2:c.1261C>G
|
XP_006713945.1:p.Arg421Gly
|
|
XM_011513459.1:c.1723C>G
|
XP_011511761.1:p.Arg575Gly
|
|
XM_011513460.1:c.1516C>G
|
XP_011511762.1:p.Arg506Gly
|
|
XM_011513461.1:c.1450C>G
|
XP_011511763.1:p.Arg484Gly
|
|
XM_011513462.1:c.1369C>G
|
XP_011511764.1:p.Arg457Gly
|
|
XM_011513463.1:c.1369C>G
|
XP_011511765.1:p.Arg457Gly
|
|
XR_924947.1:n.1913C>G
|
|
|
NM_000203.5:c.1657C>G
MANE Select
|
NP_000194.2:p.Arg553Gly
|
|
NM_001363576.1:c.1261C>G
|
NP_001350505.1:p.Arg421Gly
|
|
XM_011513461.2:c.1450C>G
|
XP_011511763.1:p.Arg484Gly
|
|
XM_017008163.1:c.697C>G
|
XP_016863652.1:p.Arg233Gly
|
|