ENST00000405460.9:c.12136T>G
MANE Select
|
ENSP00000384582.2:p.Ser4046Ala
|
|
ENST00000425867.3:c.1090T>G
|
ENSP00000392618.3:p.Ser364Ala
|
|
ENST00000639431.1:c.265+87111T>G
|
ENSP00000491057.1:n.265+87111T>G
|
|
ENST00000640464.1:n.2555T>G
|
|
|
ENST00000640729.1:n.713T>G
|
|
|
ENST00000405460.6:c.12136T>G
|
ENSP00000384582.2:p.Ser4046Ala
|
|
NM_032119.3:c.12136T>G
|
NP_115495.3:p.Ser4046Ala
|
|
NR_003149.1:n.12149T>G
|
|
|
XM_011543675.1:c.12133T>G
|
XP_011541977.1:p.Ser4045Ala
|
|
XM_011543676.1:c.12055T>G
|
XP_011541978.1:p.Ser4019Ala
|
|
XM_011543677.1:c.9439T>G
|
XP_011541979.1:p.Ser3147Ala
|
|
XM_011543678.1:c.12136T>G
|
XP_011541980.1:p.Ser4046Ala
|
|
NM_032119.4:c.12136T>G
MANE Select
|
NP_115495.3:p.Ser4046Ala
|
|
XM_017009963.2:c.12157T>G
|
XP_016865452.1:p.Ser4053Ala
|
|
XM_017009964.2:c.12154T>G
|
XP_016865453.1:p.Ser4052Ala
|
|
XM_017009965.1:c.12154T>G
|
XP_016865454.1:p.Ser4052Ala
|
|
XM_017009966.2:c.12076T>G
|
XP_016865455.1:p.Ser4026Ala
|
|
XM_017009967.1:c.12061T>G
|
XP_016865456.1:p.Ser4021Ala
|
|
XM_017009968.2:c.12157T>G
|
XP_016865457.1:p.Ser4053Ala
|
|
XM_017009969.2:c.12157T>G
|
XP_016865458.1:p.Ser4053Ala
|
|
XM_017009970.2:c.12157T>G
|
XP_016865459.1:p.Ser4053Ala
|
|
XM_017009971.2:c.12157T>G
|
XP_016865460.1:p.Ser4053Ala
|
|
XM_017009972.1:c.5275T>G
|
XP_016865461.1:p.Ser1759Ala
|
|
XM_017009973.1:c.5254T>G
|
XP_016865462.1:p.Ser1752Ala
|
|
NR_003149.2:n.12152T>G
|
|
|