ENST00000405460.9:c.11570C>A
MANE Select
|
ENSP00000384582.2:p.Ser3857Tyr
|
|
ENST00000425867.3:c.701C>A
|
ENSP00000392618.3:p.Ser234Tyr
|
|
ENST00000639431.1:c.265+78966C>A
|
ENSP00000491057.1:n.265+78966C>A
|
|
ENST00000640374.1:n.4714C>A
|
|
|
ENST00000640464.1:n.1989C>A
|
|
|
ENST00000405460.6:c.11570C>A
|
ENSP00000384582.2:p.Ser3857Tyr
|
|
ENST00000509621.1:c.4267C>A
|
|
|
NM_032119.3:c.11570C>A
|
NP_115495.3:p.Ser3857Tyr
|
|
NR_003149.1:n.11583C>A
|
|
|
XM_011543675.1:c.11567C>A
|
XP_011541977.1:p.Ser3856Tyr
|
|
XM_011543676.1:c.11489C>A
|
XP_011541978.1:p.Ser3830Tyr
|
|
XM_011543677.1:c.8873C>A
|
XP_011541979.1:p.Ser2958Tyr
|
|
XM_011543678.1:c.11570C>A
|
XP_011541980.1:p.Ser3857Tyr
|
|
NM_032119.4:c.11570C>A
MANE Select
|
NP_115495.3:p.Ser3857Tyr
|
|
XM_017009963.2:c.11591C>A
|
XP_016865452.1:p.Ser3864Tyr
|
|
XM_017009964.2:c.11588C>A
|
XP_016865453.1:p.Ser3863Tyr
|
|
XM_017009965.1:c.11588C>A
|
XP_016865454.1:p.Ser3863Tyr
|
|
XM_017009966.2:c.11510C>A
|
XP_016865455.1:p.Ser3837Tyr
|
|
XM_017009967.1:c.11495C>A
|
XP_016865456.1:p.Ser3832Tyr
|
|
XM_017009968.2:c.11591C>A
|
XP_016865457.1:p.Ser3864Tyr
|
|
XM_017009969.2:c.11591C>A
|
XP_016865458.1:p.Ser3864Tyr
|
|
XM_017009970.2:c.11591C>A
|
XP_016865459.1:p.Ser3864Tyr
|
|
XM_017009971.2:c.11591C>A
|
XP_016865460.1:p.Ser3864Tyr
|
|
XM_017009972.1:c.4709C>A
|
XP_016865461.1:p.Ser1570Tyr
|
|
XM_017009973.1:c.4688C>A
|
XP_016865462.1:p.Ser1563Tyr
|
|
NR_003149.2:n.11586C>A
|
|
|