ENST00000324862.7:c.1843+128A>C
MANE Select
|
ENSP00000315379.6:n.1843+128A>C
|
|
ENST00000324862.6:c.1843+128A>C
|
ENSP00000315379.6:n.1843+128A>C
|
|
ENST00000467329.5:n.2170+128A>C
|
|
|
ENST00000476970.1:n.952+128A>C
|
|
|
NM_004698.2:c.1843+128A>C
|
NP_004689.1:n.1843+128A>C
|
|
XM_011510128.1:c.1853+118A>C
|
XP_011508430.1:n.1853+118A>C
|
|
XM_011510129.1:c.1438+128A>C
|
XP_011508431.1:n.1438+128A>C
|
|
XM_011510130.1:c.1411+128A>C
|
XP_011508432.1:n.1411+128A>C
|
|
XR_241103.1:n.1826+128A>C
|
|
|
XR_921997.1:n.1836+118A>C
|
|
|
XR_921998.1:n.1940+128A>C
|
|
|
NM_001350529.1:c.1438+128A>C
|
NP_001337458.1:n.1438+128A>C
|
|
NM_004698.3:c.1843+128A>C
|
NP_004689.1:n.1843+128A>C
|
|
NR_146766.1:n.2074+128A>C
|
|
|
NR_146767.1:n.2170+128A>C
|
|
|
NR_146768.1:n.2026+118A>C
|
|
|
NR_146769.1:n.2079+118A>C
|
|
|
XM_011510130.3:c.1411+128A>C
|
XP_011508432.1:n.1411+128A>C
|
|
XM_017002790.1:c.1411+128A>C
|
XP_016858279.1:n.1411+128A>C
|
|
XR_001737536.2:n.1876+128A>C
|
|
|
XR_001737537.2:n.1990+128A>C
|
|
|
XR_001737540.2:n.2747+128A>C
|
|
|
XR_001737541.2:n.1770+128A>C
|
|
|
XR_002958009.1:n.2500+128A>C
|
|
|
XR_002958010.1:n.3746+118A>C
|
|
|
XR_002958012.1:n.1942+118A>C
|
|
|
XR_241103.3:n.1818+128A>C
|
|
|
XR_921997.3:n.1828+118A>C
|
|
|
XR_921998.3:n.1932+128A>C
|
|
|
NM_004698.4:c.1843+128A>C
MANE Select
|
NP_004689.1:n.1843+128A>C
|
|