ENST00000405460.9:c.12145T>G
MANE Select
|
ENSP00000384582.2:p.Ser4049Ala
|
|
ENST00000425867.3:c.1099T>G
|
ENSP00000392618.3:p.Ser367Ala
|
|
ENST00000639431.1:c.265+87120T>G
|
ENSP00000491057.1:n.265+87120T>G
|
|
ENST00000640464.1:n.2564T>G
|
|
|
ENST00000640729.1:n.722T>G
|
|
|
ENST00000405460.6:c.12145T>G
|
ENSP00000384582.2:p.Ser4049Ala
|
|
NM_032119.3:c.12145T>G
|
NP_115495.3:p.Ser4049Ala
|
|
NR_003149.1:n.12158T>G
|
|
|
XM_011543675.1:c.12142T>G
|
XP_011541977.1:p.Ser4048Ala
|
|
XM_011543676.1:c.12064T>G
|
XP_011541978.1:p.Ser4022Ala
|
|
XM_011543677.1:c.9448T>G
|
XP_011541979.1:p.Ser3150Ala
|
|
XM_011543678.1:c.12145T>G
|
XP_011541980.1:p.Ser4049Ala
|
|
NM_032119.4:c.12145T>G
MANE Select
|
NP_115495.3:p.Ser4049Ala
|
|
XM_017009963.2:c.12166T>G
|
XP_016865452.1:p.Ser4056Ala
|
|
XM_017009964.2:c.12163T>G
|
XP_016865453.1:p.Ser4055Ala
|
|
XM_017009965.1:c.12163T>G
|
XP_016865454.1:p.Ser4055Ala
|
|
XM_017009966.2:c.12085T>G
|
XP_016865455.1:p.Ser4029Ala
|
|
XM_017009967.1:c.12070T>G
|
XP_016865456.1:p.Ser4024Ala
|
|
XM_017009968.2:c.12166T>G
|
XP_016865457.1:p.Ser4056Ala
|
|
XM_017009969.2:c.12166T>G
|
XP_016865458.1:p.Ser4056Ala
|
|
XM_017009970.2:c.12166T>G
|
XP_016865459.1:p.Ser4056Ala
|
|
XM_017009971.2:c.12166T>G
|
XP_016865460.1:p.Ser4056Ala
|
|
XM_017009972.1:c.5284T>G
|
XP_016865461.1:p.Ser1762Ala
|
|
XM_017009973.1:c.5263T>G
|
XP_016865462.1:p.Ser1755Ala
|
|
NR_003149.2:n.12161T>G
|
|
|