|
ENST00000395105.9:c.1799C>T
MANE Select
|
ENSP00000378537.4:p.Ala600Val
|
|
|
ENST00000323940.9:c.1799C>T
|
ENSP00000326085.5:p.Ala600Val
|
|
|
ENST00000395105.8:c.1799C>T
|
ENSP00000378537.4:p.Ala600Val
|
|
|
ENST00000416286.7:c.1775C>T
|
ENSP00000400403.3:p.Ala592Val
|
|
|
ENST00000423167.6:c.1772C>T
|
ENSP00000413012.2:p.Ala591Val
|
|
|
ENST00000449139.6:c.1799C>T
|
ENSP00000410221.2:p.Ala600Val
|
|
|
ENST00000535552.5:c.1910C>T
|
ENSP00000440238.1:p.Ala637Val
|
|
|
ENST00000545137.5:n.1508C>T
|
|
|
|
ENST00000563965.5:c.1916C>T
|
ENSP00000456609.1:p.Ala639Val
|
|
|
ENST00000572785.1:c.654C>T
|
|
|
|
ENST00000574278.5:c.1844C>T
|
ENSP00000458827.1:p.Ala615Val
|
|
|
ENST00000574439.5:n.2071C>T
|
|
|
|
ENST00000616000.4:c.1799C>T
|
ENSP00000479112.1:p.Ala600Val
|
|
|
NM_001142617.1:c.1799C>T
|
NP_001136089.1:p.Ala600Val
|
|
|
NM_001142618.1:c.1799C>T
|
NP_001136090.1:p.Ala600Val
|
|
|
NM_001142619.1:c.1772C>T
|
NP_001136091.1:p.Ala591Val
|
|
|
NM_001199040.1:c.1910C>T
|
NP_001185969.1:p.Ala637Val
|
|
|
NM_001199041.1:c.1844C>T
|
NP_001185970.1:p.Ala615Val
|
|
|
NM_001199042.1:c.1916C>T
|
NP_001185971.1:p.Ala639Val
|
|
|
NM_022369.3:c.1799C>T
|
NP_071764.3:p.Ala600Val
|
|
|
XM_011521883.1:c.1799C>T
|
XP_011520185.1:p.Ala600Val
|
|
|
XM_011521884.1:c.1610C>T
|
XP_011520186.1:p.Ala537Val
|
|
|
XM_017022478.1:c.1847C>T
|
XP_016877967.1:p.Ala616Val
|
|
|
XM_017022479.1:c.1799C>T
|
XP_016877968.1:p.Ala600Val
|
|
|
XM_017022480.1:c.1610C>T
|
XP_016877969.1:p.Ala537Val
|
|
|
NM_022369.4:c.1799C>T
MANE Select
|
NP_071764.3:p.Ala600Val
|
|
|
NM_001142617.2:c.1799C>T
|
NP_001136089.1:p.Ala600Val
|
|
|
NM_001142619.2:c.1772C>T
|
NP_001136091.1:p.Ala591Val
|
|
|
NM_001199042.2:c.1916C>T
|
NP_001185971.1:p.Ala639Val
|
|
|
NM_001142618.2:c.1799C>T
|
NP_001136090.1:p.Ala600Val
|
|
|
NM_001199040.2:c.1910C>T
|
NP_001185969.1:p.Ala637Val
|
|
|
NM_001199041.2:c.1844C>T
|
NP_001185970.1:p.Ala615Val
|
|
