ENST00000283871.10:c.866C>T
MANE Select
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ENSP00000283871.5:p.Ala289Val
|
|
ENST00000283871.9:c.866C>T
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ENSP00000283871.5:p.Ala289Val
|
|
ENST00000470321.1:n.206C>T
|
|
|
ENST00000475447.2:c.294C>T
|
|
|
ENST00000492108.5:c.272C>T
|
ENSP00000419838.1:p.Ala91Val
|
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ENST00000494453.1:c.286C>T
|
|
|
NM_000187.3:c.866C>T
|
NP_000178.2:p.Ala289Val
|
|
XM_005247412.1:c.641C>T
|
XP_005247469.1:p.Ala214Val
|
|
XM_005247413.1:c.866C>T
|
XP_005247470.1:p.Ala289Val
|
|
XM_011512746.1:c.866C>T
|
XP_011511048.1:p.Ala289Val
|
|
XM_005247412.2:c.641C>T
|
XP_005247469.1:p.Ala214Val
|
|
XM_005247413.2:c.866C>T
|
XP_005247470.1:p.Ala289Val
|
|
XM_011512746.2:c.866C>T
|
XP_011511048.1:p.Ala289Val
|
|
XM_017006277.2:c.443C>T
|
XP_016861766.1:p.Ala148Val
|
|
NM_000187.4:c.866C>T
MANE Select
|
NP_000178.2:p.Ala289Val
|
|