|
ENST00000405460.9:c.9464C>A
MANE Select
|
ENSP00000384582.2:p.Ala3155Asp
|
|
|
ENST00000639431.1:c.265+43855C>A
|
ENSP00000491057.1:n.265+43855C>A
|
|
|
ENST00000640374.1:n.2608C>A
|
|
|
|
ENST00000640779.1:c.4193C>A
|
|
|
|
ENST00000405460.6:c.9464C>A
|
ENSP00000384582.2:p.Ala3155Asp
|
|
|
ENST00000509621.1:c.2161C>A
|
|
|
|
NM_032119.3:c.9464C>A
|
NP_115495.3:p.Ala3155Asp
|
|
|
NR_003149.1:n.9477C>A
|
|
|
|
XM_011543675.1:c.9461C>A
|
XP_011541977.1:p.Ala3154Asp
|
|
|
XM_011543676.1:c.9383C>A
|
XP_011541978.1:p.Ala3128Asp
|
|
|
XM_011543677.1:c.6767C>A
|
XP_011541979.1:p.Ala2256Asp
|
|
|
XM_011543678.1:c.9464C>A
|
XP_011541980.1:p.Ala3155Asp
|
|
|
XM_011543679.1:c.9464C>A
|
XP_011541981.1:p.Ala3155Asp
|
|
|
XR_948560.1:n.272-4255G>T
|
|
|
|
NM_032119.4:c.9464C>A
MANE Select
|
NP_115495.3:p.Ala3155Asp
|
|
|
XM_017009963.2:c.9485C>A
|
XP_016865452.1:p.Ala3162Asp
|
|
|
XM_017009964.2:c.9482C>A
|
XP_016865453.1:p.Ala3161Asp
|
|
|
XM_017009965.1:c.9482C>A
|
XP_016865454.1:p.Ala3161Asp
|
|
|
XM_017009966.2:c.9404C>A
|
XP_016865455.1:p.Ala3135Asp
|
|
|
XM_017009967.1:c.9389C>A
|
XP_016865456.1:p.Ala3130Asp
|
|
|
XM_017009968.2:c.9485C>A
|
XP_016865457.1:p.Ala3162Asp
|
|
|
XM_017009969.2:c.9485C>A
|
XP_016865458.1:p.Ala3162Asp
|
|
|
XM_017009970.2:c.9485C>A
|
XP_016865459.1:p.Ala3162Asp
|
|
|
XM_017009971.2:c.9485C>A
|
XP_016865460.1:p.Ala3162Asp
|
|
|
XM_017009972.1:c.2603C>A
|
XP_016865461.1:p.Ala868Asp
|
|
|
XM_017009973.1:c.2582C>A
|
XP_016865462.1:p.Ala861Asp
|
|
|
XM_017009974.2:c.9485C>A
|
XP_016865463.1:p.Ala3162Asp
|
|
|
XR_001742802.1:n.2523-4255G>T
|
|
|
|
NR_003149.2:n.9480C>A
|
|
|
