ENST00000405460.9:c.16301C>G
MANE Select
|
ENSP00000384582.2:p.Ser5434Ter
|
|
ENST00000425867.3:c.5255C>G
|
ENSP00000392618.3:p.Ser1752Ter
|
|
ENST00000638510.1:n.3568C>G
|
|
|
ENST00000639431.1:c.265+147320C>G
|
ENSP00000491057.1:n.265+147320C>G
|
|
ENST00000640061.1:n.128+1347C>G
|
|
|
ENST00000640407.1:c.2711C>G
|
ENSP00000491425.1:p.Ser904Ter
|
|
ENST00000405460.6:c.16301C>G
|
ENSP00000384582.2:p.Ser5434Ter
|
|
ENST00000425867.2:c.3284C>G
|
ENSP00000392618.2:p.Ser1095Ter
|
|
NM_032119.3:c.16301C>G
|
NP_115495.3:p.Ser5434Ter
|
|
NR_003149.1:n.16314C>G
|
|
|
XM_011543675.1:c.16298C>G
|
XP_011541977.1:p.Ser5433Ter
|
|
XM_011543676.1:c.16220C>G
|
XP_011541978.1:p.Ser5407Ter
|
|
XM_011543677.1:c.13604C>G
|
XP_011541979.1:p.Ser4535Ter
|
|
NM_032119.4:c.16301C>G
MANE Select
|
NP_115495.3:p.Ser5434Ter
|
|
XM_017009963.2:c.16322C>G
|
XP_016865452.1:p.Ser5441Ter
|
|
XM_017009964.2:c.16319C>G
|
XP_016865453.1:p.Ser5440Ter
|
|
XM_017009965.1:c.16319C>G
|
XP_016865454.1:p.Ser5440Ter
|
|
XM_017009966.2:c.16241C>G
|
XP_016865455.1:p.Ser5414Ter
|
|
XM_017009967.1:c.16226C>G
|
XP_016865456.1:p.Ser5409Ter
|
|
XM_017009968.2:c.16142C>G
|
XP_016865457.1:p.Ser5381Ter
|
|
XM_017009969.2:c.16322C>G
|
XP_016865458.1:p.Ser5441Ter
|
|
XM_017009972.1:c.9440C>G
|
XP_016865461.1:p.Ser3147Ter
|
|
XM_017009973.1:c.9419C>G
|
XP_016865462.1:p.Ser3140Ter
|
|
NR_003149.2:n.16317C>G
|
|
|