ENST00000642948.1:c.1707C>G
MANE Select
|
ENSP00000496347.1:p.Thr569=
|
|
ENST00000335730.6:n.1020C>G
|
|
|
ENST00000441551.6:c.1707C>G
|
ENSP00000387621.2:p.Thr569=
|
|
ENST00000536736.5:c.1707C>G
|
ENSP00000444586.1:p.Thr569=
|
|
NM_144612.6:c.1707C>G
|
NP_653213.6:p.Thr569=
|
|
XM_011525803.1:c.1707C>G
|
XP_011524105.1:p.Thr569=
|
|
XM_011525804.1:c.-30-1865C>G
|
XP_011524106.1:n.-30-1865C>G
|
|
XM_011525804.2:c.-30-1865C>G
|
XP_011524106.1:n.-30-1865C>G
|
|
XM_017025548.1:c.1707C>G
|
XP_016881037.1:p.Thr569=
|
|
XM_024451084.1:c.189C>G
|
XP_024306852.1:p.Thr63=
|
|
NM_001384474.1:c.1707C>G
MANE Select
|
NP_001371403.1:p.Thr569=
|
|
NM_144612.7:c.1707C>G
|
NP_653213.6:p.Thr569=
|
|