ENST00000358062.7:c.2249A>T
|
ENSP00000350765.3:p.Glu750Val
|
|
ENST00000682238.1:c.23A>T
|
ENSP00000508124.1:p.Glu8Val
|
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ENST00000683117.1:n.1064A>T
|
|
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ENST00000683450.1:n.986A>T
|
|
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ENST00000683851.1:n.1064A>T
|
|
|
ENST00000683957.1:n.895A>T
|
|
|
ENST00000684130.1:c.23A>T
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ENSP00000508037.1:p.Glu8Val
|
|
ENST00000357033.9:c.7403A>T
MANE Select
|
ENSP00000354923.3:p.Glu2468Val
|
|
ENST00000619831.5:c.3371A>T
|
ENSP00000479270.2:p.Glu1124Val
|
|
ENST00000620040.5:c.23A>T
|
ENSP00000478150.2:p.Glu8Val
|
|
ENST00000680961.1:c.23A>T
|
ENSP00000506386.1:p.Glu8Val
|
|
ENST00000681646.1:n.1064A>T
|
|
|
ENST00000681839.1:c.392A>T
|
ENSP00000505228.1:p.Glu131Val
|
|
ENST00000357033.8:c.7403A>T
|
ENSP00000354923.3:p.Glu2468Val
|
|
ENST00000358062.6:c.491A>T
|
ENSP00000350765.2:p.Glu164Val
|
|
ENST00000359836.5:c.23A>T
|
ENSP00000352894.1:p.Glu8Val
|
|
ENST00000378677.6:c.7391A>T
|
ENSP00000367948.2:p.Glu2464Val
|
|
ENST00000378707.7:c.23A>T
|
ENSP00000367979.3:p.Glu8Val
|
|
ENST00000471779.1:c.160A>T
|
ENSP00000417075.1:n.160A>T
|
|
ENST00000474231.5:c.23A>T
|
ENSP00000417123.1:p.Glu8Val
|
|
ENST00000541735.5:c.23A>T
|
ENSP00000444119.1:p.Glu8Val
|
|
ENST00000619831.4:c.7388A>T
|
ENSP00000479270.1:p.Glu2463Val
|
|
ENST00000620040.4:c.7400A>T
|
ENSP00000478150.1:p.Glu2467Val
|
|
NM_000109.3:c.7379A>T
|
NP_000100.2:p.Glu2460Val
|
|
NM_004006.2:c.7403A>T , LRG_199t1:c.7403A>T
|
NP_003997.1:p.Glu2468Val
|
|
NM_004009.3:c.7391A>T
|
NP_004000.1:p.Glu2464Val
|
|
NM_004010.3:c.7034A>T
|
NP_004001.1:p.Glu2345Val
|
|
NM_004011.3:c.3380A>T
|
NP_004002.2:p.Glu1127Val
|
|
NM_004012.3:c.3371A>T
|
NP_004003.1:p.Glu1124Val
|
|
NM_004013.2:c.23A>T
|
NP_004004.1:p.Glu8Val
|
|
NM_004020.3:c.23A>T
|
NP_004011.2:p.Glu8Val
|
|
NM_004021.2:c.23A>T
|
NP_004012.1:p.Glu8Val
|
|
NM_004022.2:c.23A>T
|
NP_004013.1:p.Glu8Val
|
|
NM_004023.2:c.23A>T
|
NP_004014.1:p.Glu8Val
|
|
XM_006724468.2:c.7403A>T
|
XP_006724531.1:p.Glu2468Val
|
|
XM_006724469.2:c.7379A>T
|
XP_006724532.1:p.Glu2460Val
|
|
XM_006724470.2:c.7403A>T
|
XP_006724533.1:p.Glu2468Val
|
|
XM_006724471.2:c.7403A>T
|
XP_006724534.1:p.Glu2468Val
|
|
XM_006724472.2:c.7274A>T
|
XP_006724535.1:p.Glu2425Val
|
|
XM_006724473.2:c.7265A>T
|
XP_006724536.1:p.Glu2422Val
|
|
XM_006724474.2:c.7403A>T
|
XP_006724537.1:p.Glu2468Val
|
|
XM_006724475.2:c.7403A>T
|
XP_006724538.1:p.Glu2468Val
|
|
XM_011545467.1:c.7280A>T
|
XP_011543769.1:p.Glu2427Val
|
|
XM_011545468.1:c.7403A>T
|
XP_011543770.1:p.Glu2468Val
|
|
XM_006724469.3:c.7379A>T
|
XP_006724532.1:p.Glu2460Val
|
|
XM_006724470.3:c.7403A>T
|
XP_006724533.1:p.Glu2468Val
|
|
XM_006724474.3:c.7403A>T
|
XP_006724537.1:p.Glu2468Val
|
|
XM_011545468.2:c.7403A>T
|
XP_011543770.1:p.Glu2468Val
|
|
XM_017029328.1:c.7403A>T
|
XP_016884817.1:p.Glu2468Val
|
|
XM_017029331.1:c.1577A>T
|
XP_016884820.1:p.Glu526Val
|
|
NM_000109.4:c.7379A>T
|
NP_000100.3:p.Glu2460Val
|
|
NM_004006.3:c.7403A>T
MANE Select
|
NP_003997.2:p.Glu2468Val
|
|
NM_004011.4:c.3380A>T
|
NP_004002.3:p.Glu1127Val
|
|
NM_004012.4:c.3371A>T
|
NP_004003.2:p.Glu1124Val
|
|
NM_004021.3:c.23A>T
|
NP_004012.2:p.Glu8Val
|
|
NM_004023.3:c.23A>T
|
NP_004014.2:p.Glu8Val
|
|
NM_004013.3:c.23A>T
|
NP_004004.2:p.Glu8Val
|
|
NM_004020.4:c.23A>T
|
NP_004011.3:p.Glu8Val
|
|
NM_004022.3:c.23A>T
|
NP_004013.2:p.Glu8Val
|
|