ENST00000405460.9:c.11441T>G
MANE Select
|
ENSP00000384582.2:p.Ile3814Ser
|
|
ENST00000425867.3:c.572T>G
|
ENSP00000392618.3:p.Ile191Ser
|
|
ENST00000639431.1:c.265+78837T>G
|
ENSP00000491057.1:n.265+78837T>G
|
|
ENST00000640374.1:n.4585T>G
|
|
|
ENST00000640464.1:n.1860T>G
|
|
|
ENST00000405460.6:c.11441T>G
|
ENSP00000384582.2:p.Ile3814Ser
|
|
ENST00000509621.1:c.4138T>G
|
|
|
NM_032119.3:c.11441T>G
|
NP_115495.3:p.Ile3814Ser
|
|
NR_003149.1:n.11454T>G
|
|
|
XM_011543675.1:c.11438T>G
|
XP_011541977.1:p.Ile3813Ser
|
|
XM_011543676.1:c.11360T>G
|
XP_011541978.1:p.Ile3787Ser
|
|
XM_011543677.1:c.8744T>G
|
XP_011541979.1:p.Ile2915Ser
|
|
XM_011543678.1:c.11441T>G
|
XP_011541980.1:p.Ile3814Ser
|
|
NM_032119.4:c.11441T>G
MANE Select
|
NP_115495.3:p.Ile3814Ser
|
|
XM_017009963.2:c.11462T>G
|
XP_016865452.1:p.Ile3821Ser
|
|
XM_017009964.2:c.11459T>G
|
XP_016865453.1:p.Ile3820Ser
|
|
XM_017009965.1:c.11459T>G
|
XP_016865454.1:p.Ile3820Ser
|
|
XM_017009966.2:c.11381T>G
|
XP_016865455.1:p.Ile3794Ser
|
|
XM_017009967.1:c.11366T>G
|
XP_016865456.1:p.Ile3789Ser
|
|
XM_017009968.2:c.11462T>G
|
XP_016865457.1:p.Ile3821Ser
|
|
XM_017009969.2:c.11462T>G
|
XP_016865458.1:p.Ile3821Ser
|
|
XM_017009970.2:c.11462T>G
|
XP_016865459.1:p.Ile3821Ser
|
|
XM_017009971.2:c.11462T>G
|
XP_016865460.1:p.Ile3821Ser
|
|
XM_017009972.1:c.4580T>G
|
XP_016865461.1:p.Ile1527Ser
|
|
XM_017009973.1:c.4559T>G
|
XP_016865462.1:p.Ile1520Ser
|
|
NR_003149.2:n.11457T>G
|
|
|