ENST00000405460.9:c.12155C>A
MANE Select
|
ENSP00000384582.2:p.Pro4052His
|
|
ENST00000425867.3:c.1109C>A
|
ENSP00000392618.3:p.Pro370His
|
|
ENST00000639431.1:c.265+87130C>A
|
ENSP00000491057.1:n.265+87130C>A
|
|
ENST00000640464.1:n.2574C>A
|
|
|
ENST00000640729.1:n.732C>A
|
|
|
ENST00000405460.6:c.12155C>A
|
ENSP00000384582.2:p.Pro4052His
|
|
NM_032119.3:c.12155C>A
|
NP_115495.3:p.Pro4052His
|
|
NR_003149.1:n.12168C>A
|
|
|
XM_011543675.1:c.12152C>A
|
XP_011541977.1:p.Pro4051His
|
|
XM_011543676.1:c.12074C>A
|
XP_011541978.1:p.Pro4025His
|
|
XM_011543677.1:c.9458C>A
|
XP_011541979.1:p.Pro3153His
|
|
XM_011543678.1:c.12155C>A
|
XP_011541980.1:p.Pro4052His
|
|
NM_032119.4:c.12155C>A
MANE Select
|
NP_115495.3:p.Pro4052His
|
|
XM_017009963.2:c.12176C>A
|
XP_016865452.1:p.Pro4059His
|
|
XM_017009964.2:c.12173C>A
|
XP_016865453.1:p.Pro4058His
|
|
XM_017009965.1:c.12173C>A
|
XP_016865454.1:p.Pro4058His
|
|
XM_017009966.2:c.12095C>A
|
XP_016865455.1:p.Pro4032His
|
|
XM_017009967.1:c.12080C>A
|
XP_016865456.1:p.Pro4027His
|
|
XM_017009968.2:c.12176C>A
|
XP_016865457.1:p.Pro4059His
|
|
XM_017009969.2:c.12176C>A
|
XP_016865458.1:p.Pro4059His
|
|
XM_017009970.2:c.12176C>A
|
XP_016865459.1:p.Pro4059His
|
|
XM_017009971.2:c.12176C>A
|
XP_016865460.1:p.Pro4059His
|
|
XM_017009972.1:c.5294C>A
|
XP_016865461.1:p.Pro1765His
|
|
XM_017009973.1:c.5273C>A
|
XP_016865462.1:p.Pro1758His
|
|
NR_003149.2:n.12171C>A
|
|
|