ENST00000389857.11:c.5107G>T
MANE Select
|
ENSP00000374507.6:p.Ala1703Ser
|
|
ENST00000331194.8:c.679G>T
|
ENSP00000330332.8:p.Ala227Ser
|
|
ENST00000334448.5:n.919G>T
|
|
|
ENST00000389857.10:c.5107G>T
|
ENSP00000374507.6:p.Ala1703Ser
|
|
ENST00000556726.5:c.1335G>T
|
|
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NM_001080414.3:c.5107G>T
|
NP_001073883.2:p.Ala1703Ser
|
|
XM_011536796.1:c.4999G>T
|
XP_011535098.1:p.Ala1667Ser
|
|
XR_429316.2:n.5382G>T
|
|
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XM_011536796.2:c.4999G>T
|
XP_011535098.1:p.Ala1667Ser
|
|
XM_017021336.1:c.2188G>T
|
XP_016876825.1:p.Ala730Ser
|
|
XR_429316.4:n.5380G>T
|
|
|
NM_001080414.4:c.5107G>T
MANE Select
|
NP_001073883.2:p.Ala1703Ser
|
|