ENST00000438166.7:c.1877A>T
MANE Select
|
ENSP00000409708.2:p.Asp626Val
|
|
ENST00000310454.10:c.1877A>T
|
ENSP00000308610.5:p.Asp626Val
|
|
ENST00000409125.8:c.1499A>T
|
ENSP00000386484.5:p.Asp500Val
|
|
ENST00000409674.5:c.1877A>T
|
ENSP00000386425.1:p.Asp626Val
|
|
ENST00000409861.5:c.1877A>T
|
ENSP00000386626.1:p.Asp626Val
|
|
ENST00000438166.6:c.1877A>T
|
ENSP00000409708.2:p.Asp626Val
|
|
ENST00000464846.5:n.231A>T
|
|
|
ENST00000540309.5:c.1135-88A>T
|
ENSP00000440892.1:n.1135-88A>T
|
|
NM_000408.4:c.1877A>T
|
NP_000399.3:p.Asp626Val
|
|
NM_001083112.2:c.1877A>T
|
NP_001076581.2:p.Asp626Val
|
|
XM_005246469.1:c.1877A>T
|
XP_005246526.1:p.Asp626Val
|
|
XM_005246470.3:c.1775A>T
|
XP_005246527.1:p.Asp592Val
|
|
XM_011510977.1:c.1877A>T
|
XP_011509279.1:p.Asp626Val
|
|
XM_011510978.1:c.1775A>T
|
XP_011509280.1:p.Asp592Val
|
|
XM_011510979.1:c.1499A>T
|
XP_011509281.1:p.Asp500Val
|
|
XM_011510980.1:c.1196A>T
|
XP_011509282.1:p.Asp399Val
|
|
XM_005246469.2:c.1877A>T
|
XP_005246526.1:p.Asp626Val
|
|
XM_011510977.2:c.1877A>T
|
XP_011509279.1:p.Asp626Val
|
|
XM_011510978.2:c.1775A>T
|
XP_011509280.1:p.Asp592Val
|
|
XM_017003830.1:c.1877A>T
|
XP_016859319.1:p.Asp626Val
|
|
XM_024452798.1:c.1877A>T
|
XP_024308566.1:p.Asp626Val
|
|
NM_000408.5:c.1877A>T
MANE Select
|
NP_000399.3:p.Asp626Val
|
|
NM_001083112.3:c.1877A>T
|
NP_001076581.2:p.Asp626Val
|
|