ENST00000367099.4:n.1513G>T
|
|
|
ENST00000471071.2:c.253G>T
|
ENSP00000493073.2:p.Ala85Ser
|
|
ENST00000640756.2:n.318G>T
|
|
|
ENST00000659065.2:c.391G>T
|
ENSP00000499588.1:p.Ala131Ser
|
|
ENST00000659642.2:c.391G>T
|
ENSP00000499509.1:p.Ala131Ser
|
|
ENST00000664374.2:c.391G>T
|
ENSP00000499664.1:p.Ala131Ser
|
|
ENST00000640756.1:n.307G>T
|
|
|
ENST00000659065.1:c.391G>T
|
ENSP00000499588.1:p.Ala131Ser
|
|
ENST00000659642.1:c.391G>T
|
ENSP00000499509.1:p.Ala131Ser
|
|
ENST00000664374.1:c.391G>T
|
ENSP00000499664.1:p.Ala131Ser
|
|
ENST00000423557.1:c.508G>T
MANE Select
|
ENSP00000412237.1:p.Ala170Ser
|
|
NM_000572.2:c.508G>T
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NP_000563.1:p.Ala170Ser
|
|
XM_011509506.1:c.508G>T
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XP_011507808.1:p.Ala170Ser
|
|
NM_000572.3:c.508G>T
MANE Select
|
NP_000563.1:p.Ala170Ser
|
|
NM_001382624.1:c.253G>T
|
NP_001369553.1:p.Ala85Ser
|
|
NR_168466.1:n.805G>T
|
|
|
NR_168467.1:n.335G>T
|
|
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