ENST00000405460.9:c.10083T>G
MANE Select
|
ENSP00000384582.2:p.Ser3361=
|
|
ENST00000639431.1:c.265+49369T>G
|
ENSP00000491057.1:n.265+49369T>G
|
|
ENST00000640374.1:n.3227T>G
|
|
|
ENST00000640464.1:n.502T>G
|
|
|
ENST00000405460.6:c.10083T>G
|
ENSP00000384582.2:p.Ser3361=
|
|
ENST00000509621.1:c.2780T>G
|
|
|
NM_032119.3:c.10083T>G
|
NP_115495.3:p.Ser3361=
|
|
NR_003149.1:n.10096T>G
|
|
|
XM_011543675.1:c.10080T>G
|
XP_011541977.1:p.Ser3360=
|
|
XM_011543676.1:c.10002T>G
|
XP_011541978.1:p.Ser3334=
|
|
XM_011543677.1:c.7386T>G
|
XP_011541979.1:p.Ser2462=
|
|
XM_011543678.1:c.10083T>G
|
XP_011541980.1:p.Ser3361=
|
|
XM_011543679.1:c.10083T>G
|
XP_011541981.1:p.Ser3361=
|
|
XR_948560.1:n.272-9769A>C
|
|
|
NM_032119.4:c.10083T>G
MANE Select
|
NP_115495.3:p.Ser3361=
|
|
XM_017009963.2:c.10104T>G
|
XP_016865452.1:p.Ser3368=
|
|
XM_017009964.2:c.10101T>G
|
XP_016865453.1:p.Ser3367=
|
|
XM_017009965.1:c.10101T>G
|
XP_016865454.1:p.Ser3367=
|
|
XM_017009966.2:c.10023T>G
|
XP_016865455.1:p.Ser3341=
|
|
XM_017009967.1:c.10008T>G
|
XP_016865456.1:p.Ser3336=
|
|
XM_017009968.2:c.10104T>G
|
XP_016865457.1:p.Ser3368=
|
|
XM_017009969.2:c.10104T>G
|
XP_016865458.1:p.Ser3368=
|
|
XM_017009970.2:c.10104T>G
|
XP_016865459.1:p.Ser3368=
|
|
XM_017009971.2:c.10104T>G
|
XP_016865460.1:p.Ser3368=
|
|
XM_017009972.1:c.3222T>G
|
XP_016865461.1:p.Ser1074=
|
|
XM_017009973.1:c.3201T>G
|
XP_016865462.1:p.Ser1067=
|
|
XM_017009974.2:c.10104T>G
|
XP_016865463.1:p.Ser3368=
|
|
XR_001742802.1:n.2523-9769A>C
|
|
|
NR_003149.2:n.10099T>G
|
|
|