|
ENST00000646891.2:c.1781_1798dup
MANE Select
|
ENSP00000493543.1:p.Thr599_Val600insAspPh...
|
|
|
ENST00000288602.11:c.1901_1918dup
|
ENSP00000288602.7:p.Thr639_Val640insAspPh...
|
|
|
ENST00000479537.6:c.451_468dup
|
|
|
|
ENST00000496384.7:c.1781_1798dup
|
ENSP00000419060.2:p.Thr599_Val600insAspPh...
|
|
|
ENST00000497784.2:c.*1231_*1248dup
|
ENSP00000420119.2:n.*1231_*1248dup
|
|
|
ENST00000642228.1:c.*859_*876dup
|
ENSP00000493678.1:n.*859_*876dup
|
|
|
ENST00000642875.1:n.1259-3936_1259-3919dup
|
|
|
|
ENST00000644120.1:n.2171_2188dup
|
|
|
|
ENST00000644650.1:c.877_894dup
|
|
|
|
ENST00000644905.1:n.2663_2680dup
|
|
|
|
ENST00000644969.2:c.1901_1918dup
MANE Plus Clinical
|
ENSP00000496776.1:p.Thr639_Val640insAspPh...
|
|
|
ENST00000646730.1:c.*357_*374dup
|
ENSP00000494784.1:n.*357_*374dup
|
|
|
ENST00000646891.1:c.1781_1798dup
|
ENSP00000493543.1:p.Thr599_Val600insAspPh...
|
|
|
ENST00000647434.1:c.738-3936_738-3919dup
|
ENSP00000495132.1:n.738-3936_738-3919dup
|
|
|
ENST00000288602.10:c.1781_1798dup
|
ENSP00000288602.6:p.Thr599_Val600insAspPh...
|
|
|
ENST00000479537.5:c.65_82dup
|
ENSP00000418033.1:p.Thr27_Val28insAspPheG...
|
|
|
ENST00000496384.6:c.604_621dup
|
|
|
|
ENST00000497784.1:c.1816_1833dup
|
ENSP00000420119.1:n.1816_1833dup
|
|
|
NM_004333.4:c.1781_1798dup , LRG_299t1:c.1781_1798dup
|
NP_004324.2:p.Thr599_Val600insAspPheGlyLe...
|
|
|
XM_005250045.1:c.1781_1798dup
|
XP_005250102.1:p.Thr599_Val600insAspPheGl...
|
|
|
XM_005250046.1:c.1781_1798dup
|
XP_005250103.1:p.Thr599_Val600insAspPheGl...
|
|
|
XM_011516529.1:c.1781_1798dup
|
XP_011514831.1:p.Thr599_Val600insAspPheGl...
|
|
|
XM_011516530.1:c.1695-3936_1695-3919dup
|
XP_011514832.1:n.1695-3936_1695-3919dup
|
|
|
XR_242190.1:n.1789_1806dup
|
|
|
|
XR_927520.1:n.1789_1806dup
|
|
|
|
XR_927521.1:n.1789_1806dup
|
|
|
|
XR_927522.1:n.1703-3936_1703-3919dup
|
|
|
|
XR_927523.1:n.1703-3936_1703-3919dup
|
|
|
|
NM_001354609.1:c.1781_1798dup
|
NP_001341538.1:p.Thr599_Val600insAspPheGl...
|
|
|
NM_004333.5:c.1781_1798dup
|
NP_004324.2:p.Thr599_Val600insAspPheGlyLe...
|
|
|
NR_148928.1:n.2879_2896dup
|
|
|
|
XM_017012558.1:c.1901_1918dup
|
XP_016868047.1:p.Thr639_Val640insAspPheGl...
|
|
|
XM_017012559.1:c.1901_1918dup
|
XP_016868048.1:p.Thr639_Val640insAspPheGl...
|
|
|
XR_001744857.1:n.1909_1926dup
|
|
|
|
XR_001744858.1:n.1823-3936_1823-3919dup
|
|
|
|
NM_001354609.2:c.1781_1798dup
|
NP_001341538.1:p.Thr599_Val600insAspPheGl...
|
|
|
NM_001374244.1:c.1901_1918dup
|
NP_001361173.1:p.Thr639_Val640insAspPheGl...
|
|
|
NM_001374258.1:c.1901_1918dup
MANE Plus Clinical
|
NP_001361187.1:p.Thr639_Val640insAspPheGl...
|
|
|
NM_004333.6:c.1781_1798dup
MANE Select
|
NP_004324.2:p.Thr599_Val600insAspPheGlyLe...
|
|
|
NM_001378467.1:c.1790_1807dup
|
NP_001365396.1:p.Thr602_Val603insAspPheGl...
|
|
|
NM_001378468.1:c.1781_1798dup
|
NP_001365397.1:p.Thr599_Val600insAspPheGl...
|
|
|
NM_001378469.1:c.1715_1732dup
|
NP_001365398.1:p.Thr577_Val578insAspPheGl...
|
|
|
NM_001378470.1:c.1679_1696dup
|
NP_001365399.1:p.Thr565_Val566insAspPheGl...
|
|
|
NM_001378471.1:c.1670_1687dup
|
NP_001365400.1:p.Thr562_Val563insAspPheGl...
|
|
|
NM_001378472.1:c.1625_1642dup
|
NP_001365401.1:p.Thr547_Val548insAspPheGl...
|
|
|
NM_001378473.1:c.1625_1642dup
|
NP_001365402.1:p.Thr547_Val548insAspPheGl...
|
|
|
NM_001378474.1:c.1781_1798dup
|
NP_001365403.1:p.Thr599_Val600insAspPheGl...
|
|
|
NM_001378475.1:c.1517_1534dup
|
NP_001365404.1:p.Thr511_Val512insAspPheGl...
|
|
