ENST00000355265.7:c.578C>G
MANE Select
|
ENSP00000347409.2:p.Thr193Arg
|
|
ENST00000467543.6:c.*430C>G
|
ENSP00000420011.2:n.*430C>G
|
|
ENST00000355265.6:c.578C>G
|
ENSP00000347409.2:p.Thr193Arg
|
|
ENST00000467543.5:c.521C>G
|
ENSP00000420011.1:p.Thr174Arg
|
|
ENST00000476829.5:c.525+383C>G
|
ENSP00000419889.1:n.525+383C>G
|
|
ENST00000479768.6:n.696C>G
|
|
|
ENST00000494148.1:n.177C>G
|
|
|
NM_000420.2:c.578C>G
|
NP_000411.1:p.Thr193Arg
|
|
XM_005249993.2:c.614C>G
|
XP_005250050.1:p.Thr205Arg
|
|
NM_000420.3:c.578C>G
MANE Select
|
NP_000411.1:p.Thr193Arg
|
|