|
NM_024753.5:c.3112G>T
MANE Select
|
NP_079029.3:p.Glu1038Ter
|
|
ENST00000243344.8:c.3112G>T
MANE Select
|
ENSP00000243344.7:p.Glu1038Ter
|
|
NM_024753.4:c.3112G>T
|
NP_079029.3:p.Glu1038Ter
|
|
ENST00000243344.7:c.3112G>T
|
ENSP00000243344.7:p.Glu1038Ter
|
|
ENST00000392695.6:c.12G>T
|
|
|
ENST00000652557.1:c.3112G>T
|
ENSP00000498617.1:p.Glu1038Ter
|
|
ENST00000679356.1:c.3112G>T
|
ENSP00000506245.1:p.Glu1038Ter
|
|
ENST00000679676.1:c.3001G>T
|
ENSP00000505492.1:p.Glu1001Ter
|
|
ENST00000679799.1:c.3112G>T
|
ENSP00000505208.1:p.Glu1038Ter
|
|
ENST00000679840.1:c.3112G>T
|
ENSP00000505248.1:p.Glu1038Ter
|
|
ENST00000679931.1:c.*2154G>T
|
ENSP00000505632.1:n.*2154G>T
|
|
ENST00000679967.1:c.3103G>T
|
ENSP00000506607.1:p.Glu1035Ter
|
|
ENST00000680327.1:c.*2154G>T
|
ENSP00000506639.1:n.*2154G>T
|
|
ENST00000680657.1:n.3223G>T
|
|
|
ENST00000680690.1:c.*2364G>T
|
ENSP00000506121.1:n.*2364G>T
|
|
ENST00000680888.1:c.3112G>T
|
ENSP00000506276.1:p.Glu1038Ter
|
|
ENST00000680925.1:n.1142G>T
|
|
|
ENST00000680947.1:c.*2384G>T
|
ENSP00000506496.1:n.*2384G>T
|
|
ENST00000681024.1:c.3112G>T
|
ENSP00000506449.1:p.Glu1038Ter
|
|
ENST00000681083.1:c.*2846G>T
|
ENSP00000506095.1:n.*2846G>T
|
|
ENST00000681167.1:n.2986G>T
|
|
|
ENST00000681483.1:c.3072G>T
|
ENSP00000505499.1:p.Glu1024Asp
|
|
ENST00000681502.1:c.*6372G>T
|
ENSP00000505644.1:n.*6372G>T
|
|
ENST00000681819.1:c.3069G>T
|
ENSP00000505673.1:p.Glu1023Asp
|
|
ENST00000681952.1:c.3112G>T
|
ENSP00000506400.1:p.Glu1038Ter
|
|
XM_011511870.1:c.2545G>T
|
XP_011510172.1:p.Glu849Ter
|
|
XM_011511871.1:c.2362G>T
|
XP_011510173.1:p.Glu788Ter
|
|
XM_011511871.3:c.2362G>T
|
XP_011510173.1:p.Glu788Ter
|
|
XM_011511872.1:c.*314G>T
|
XP_011510174.1:n.*314G>T
|
|
XM_011511872.2:c.*314G>T
|
XP_011510174.1:n.*314G>T
|
|
XM_017004967.1:c.3112G>T
|
XP_016860456.1:p.Glu1038Ter
|
|
XM_017004968.2:c.2458G>T
|
XP_016860457.1:p.Glu820Ter
|
|
XM_017004969.1:c.2113G>T
|
XP_016860458.1:p.Glu705Ter
|
