ENST00000681999.1:n.319G>A
|
|
|
ENST00000682451.1:n.291G>A
|
|
|
ENST00000682975.1:n.337G>A
|
|
|
ENST00000683894.1:c.190G>A
|
ENSP00000507789.1:p.Ala64Thr
|
|
ENST00000684085.1:n.319G>A
|
|
|
ENST00000684712.1:n.550G>A
|
|
|
ENST00000403359.8:c.442G>A
MANE Select
|
ENSP00000384823.4:p.Ala148Thr
|
|
ENST00000316377.8:c.208G>A
|
ENSP00000323822.5:p.Ala70Thr
|
|
ENST00000402508.5:c.190G>A
|
ENSP00000385398.1:p.Ala64Thr
|
|
ENST00000403359.7:c.442G>A
|
ENSP00000384823.3:p.Ala148Thr
|
|
ENST00000424163.2:c.190G>A
|
ENSP00000392272.1:p.Ala64Thr
|
|
ENST00000480038.1:n.405G>A
|
|
|
ENST00000492225.5:n.290G>A
|
|
|
NM_001190274.1:c.442G>A
|
NP_001177203.1:p.Ala148Thr
|
|
NM_025133.4:c.190G>A
|
NP_079409.3:p.Ala64Thr
|
|
XM_005264572.3:c.442G>A
|
XP_005264629.1:p.Ala148Thr
|
|
XM_005264573.3:c.442G>A
|
XP_005264630.1:p.Ala148Thr
|
|
XM_005264572.5:c.442G>A
|
XP_005264629.1:p.Ala148Thr
|
|
XM_005264573.5:c.442G>A
|
XP_005264630.1:p.Ala148Thr
|
|
XM_017005015.1:c.442G>A
|
XP_016860504.1:p.Ala148Thr
|
|
XM_017005016.2:c.190G>A
|
XP_016860505.1:p.Ala64Thr
|
|
XM_017005017.1:c.190G>A
|
XP_016860506.1:p.Ala64Thr
|
|
NM_001190274.2:c.442G>A
MANE Select
|
NP_001177203.1:p.Ala148Thr
|
|
NM_001374325.1:c.190G>A
|
NP_001361254.1:p.Ala64Thr
|
|