ENST00000405460.9:c.9128T>C
MANE Select
|
ENSP00000384582.2:p.Phe3043Ser
|
|
ENST00000639431.1:c.265+36163T>C
|
ENSP00000491057.1:n.265+36163T>C
|
|
ENST00000639473.1:n.4587T>C
|
|
|
ENST00000640012.1:c.2935T>C
|
|
|
ENST00000640374.1:n.2272T>C
|
|
|
ENST00000640779.1:c.3857T>C
|
|
|
ENST00000405460.6:c.9128T>C
|
ENSP00000384582.2:p.Phe3043Ser
|
|
ENST00000509621.1:c.1825T>C
|
|
|
NM_032119.3:c.9128T>C
|
NP_115495.3:p.Phe3043Ser
|
|
NR_003149.1:n.9141T>C
|
|
|
XM_011543675.1:c.9125T>C
|
XP_011541977.1:p.Phe3042Ser
|
|
XM_011543676.1:c.9047T>C
|
XP_011541978.1:p.Phe3016Ser
|
|
XM_011543677.1:c.6431T>C
|
XP_011541979.1:p.Phe2144Ser
|
|
XM_011543678.1:c.9128T>C
|
XP_011541980.1:p.Phe3043Ser
|
|
XM_011543679.1:c.9128T>C
|
XP_011541981.1:p.Phe3043Ser
|
|
NM_032119.4:c.9128T>C
MANE Select
|
NP_115495.3:p.Phe3043Ser
|
|
XM_017009963.2:c.9149T>C
|
XP_016865452.1:p.Phe3050Ser
|
|
XM_017009964.2:c.9146T>C
|
XP_016865453.1:p.Phe3049Ser
|
|
XM_017009965.1:c.9146T>C
|
XP_016865454.1:p.Phe3049Ser
|
|
XM_017009966.2:c.9068T>C
|
XP_016865455.1:p.Phe3023Ser
|
|
XM_017009967.1:c.9053T>C
|
XP_016865456.1:p.Phe3018Ser
|
|
XM_017009968.2:c.9149T>C
|
XP_016865457.1:p.Phe3050Ser
|
|
XM_017009969.2:c.9149T>C
|
XP_016865458.1:p.Phe3050Ser
|
|
XM_017009970.2:c.9149T>C
|
XP_016865459.1:p.Phe3050Ser
|
|
XM_017009971.2:c.9149T>C
|
XP_016865460.1:p.Phe3050Ser
|
|
XM_017009972.1:c.2267T>C
|
XP_016865461.1:p.Phe756Ser
|
|
XM_017009973.1:c.2246T>C
|
XP_016865462.1:p.Phe749Ser
|
|
XM_017009974.2:c.9149T>C
|
XP_016865463.1:p.Phe3050Ser
|
|
NR_003149.2:n.9144T>C
|
|
|