|
ENST00000455125.2:c.866C>T
|
ENSP00000390154.2:p.Ala289Val
|
|
|
ENST00000456894.6:c.728C>T
|
ENSP00000415588.3:p.Ala243Val
|
|
|
ENST00000689035.1:c.866C>T
MANE Select
|
ENSP00000508608.1:p.Ala289Val
|
|
|
ENST00000690927.1:c.854+12C>T
|
ENSP00000508791.1:n.854+12C>T
|
|
|
ENST00000405018.5:c.929C>T
|
ENSP00000385616.1:p.Ala310Val
|
|
|
ENST00000405510.5:c.866C>T
|
ENSP00000385740.1:p.Ala289Val
|
|
|
ENST00000406622.5:c.866C>T
|
ENSP00000383992.1:p.Ala289Val
|
|
|
ENST00000464202.1:n.76C>T
|
|
|
|
NM_001199579.1:c.929C>T
|
NP_001186508.1:p.Ala310Val
|
|
|
NM_001199580.1:c.866C>T
|
NP_001186509.1:p.Ala289Val
|
|
|
NM_015374.2:c.866C>T
|
NP_056189.1:p.Ala289Val
|
|
|
XM_011530104.1:c.728C>T
|
XP_011528406.1:p.Ala243Val
|
|
|
XM_011530105.1:c.833C>T
|
XP_011528407.1:p.Ala278Val
|
|
|
XM_011530104.2:c.728C>T
|
XP_011528406.1:p.Ala243Val
|
|
|
XM_011530105.2:c.833C>T
|
XP_011528407.1:p.Ala278Val
|
|
|
XM_017028748.1:c.866C>T
|
XP_016884237.1:p.Ala289Val
|
|
|
XM_024452203.1:c.1145C>T
|
XP_024307971.1:p.Ala382Val
|
|
|
XM_024452204.1:c.971C>T
|
XP_024307972.1:p.Ala324Val
|
|
|
XM_024452205.1:c.866C>T
|
XP_024307973.1:p.Ala289Val
|
|
|
XM_024452206.1:c.728C>T
|
XP_024307974.1:p.Ala243Val
|
|
|
NM_001199579.2:c.929C>T
|
NP_001186508.1:p.Ala310Val
|
|
|
NM_001199580.2:c.866C>T
|
NP_001186509.1:p.Ala289Val
|
|
|
NM_015374.3:c.866C>T
MANE Select
|
NP_056189.1:p.Ala289Val
|
|
|
NM_001394427.1:c.959C>T
|
NP_001381356.1:p.Ala320Val
|
|
|
NM_001394428.1:c.929C>T
|
NP_001381357.1:p.Ala310Val
|
|
|
NM_001394429.1:c.911C>T
|
NP_001381358.1:p.Ala304Val
|
|
|
NM_001394430.1:c.911C>T
|
NP_001381359.1:p.Ala304Val
|
|
|
NM_001394431.1:c.866C>T
|
NP_001381360.1:p.Ala289Val
|
|
|
NM_001394432.1:c.866C>T
|
NP_001381361.1:p.Ala289Val
|
|
|
NM_001394433.1:c.866C>T
|
NP_001381362.1:p.Ala289Val
|
|
|
NM_001394434.1:c.866C>T
|
NP_001381363.1:p.Ala289Val
|
|
|
NM_001394435.1:c.866C>T
|
NP_001381364.1:p.Ala289Val
|
|
|
NM_001394436.1:c.866C>T
|
NP_001381365.1:p.Ala289Val
|
|
|
NM_001394437.1:c.866C>T
|
NP_001381366.1:p.Ala289Val
|
|
|
NM_001394438.1:c.776C>T
|
NP_001381367.1:p.Ala259Val
|
|
|
NM_001394439.1:c.728C>T
|
NP_001381368.1:p.Ala243Val
|
|
|
NM_001394440.1:c.728C>T
|
NP_001381369.1:p.Ala243Val
|
|
|
NM_001394441.1:c.728C>T
|
NP_001381370.1:p.Ala243Val
|
|
|
NM_001394442.1:c.814-2093C>T
|
NP_001381371.1:n.814-2093C>T
|
|
|
NM_001394443.1:c.374C>T
|
NP_001381372.1:p.Ala125Val
|
|
|
NM_001394444.1:c.615-2071C>T
|
NP_001381373.1:n.615-2071C>T
|
|
|
NM_001394445.1:c.615-2071C>T
|
NP_001381374.1:n.615-2071C>T
|
|
