ENST00000405460.9:c.16270G=
MANE Select
|
ENSP00000384582.2:p.Val5424=
|
|
ENST00000425867.3:c.5224G=
|
ENSP00000392618.3:p.Val1742=
|
|
ENST00000638510.1:n.3537G=
|
|
|
ENST00000639431.1:c.265+147289G=
|
ENSP00000491057.1:n.265+147289G=
|
|
ENST00000640061.1:n.128+1316G=
|
|
|
ENST00000640407.1:c.2680G=
|
ENSP00000491425.1:p.Val894=
|
|
ENST00000405460.6:c.16270G=
|
ENSP00000384582.2:p.Val5424=
|
|
ENST00000425867.2:c.3253G=
|
ENSP00000392618.2:p.Val1085=
|
|
NM_032119.3:c.16270G=
|
NP_115495.3:p.Val5424=
|
|
NR_003149.1:n.16283G=
|
|
|
XM_011543675.1:c.16267G=
|
XP_011541977.1:p.Val5423=
|
|
XM_011543676.1:c.16189G=
|
XP_011541978.1:p.Val5397=
|
|
XM_011543677.1:c.13573G=
|
XP_011541979.1:p.Val4525=
|
|
NM_032119.4:c.16270G=
MANE Select
|
NP_115495.3:p.Val5424=
|
|
XM_017009963.2:c.16291G=
|
XP_016865452.1:p.Val5431=
|
|
XM_017009964.2:c.16288G=
|
XP_016865453.1:p.Val5430=
|
|
XM_017009965.1:c.16288G=
|
XP_016865454.1:p.Val5430=
|
|
XM_017009966.2:c.16210G=
|
XP_016865455.1:p.Val5404=
|
|
XM_017009967.1:c.16195G=
|
XP_016865456.1:p.Val5399=
|
|
XM_017009968.2:c.16111G=
|
XP_016865457.1:p.Val5371=
|
|
XM_017009969.2:c.16291G=
|
XP_016865458.1:p.Val5431=
|
|
XM_017009972.1:c.9409G=
|
XP_016865461.1:p.Val3137=
|
|
XM_017009973.1:c.9388G=
|
XP_016865462.1:p.Val3130=
|
|
NR_003149.2:n.16286G=
|
|
|