ENST00000527168.6:n.898G>A
|
|
|
ENST00000529110.2:c.883G>A
|
ENSP00000435349.2:p.Gly295Ser
|
|
ENST00000529957.6:n.857G>A
|
|
|
ENST00000683366.1:c.*531G>A
|
ENSP00000507283.1:n.*531G>A
|
|
ENST00000683887.1:c.847G>A
|
ENSP00000506886.1:p.Gly283Ser
|
|
ENST00000684100.1:n.793G>A
|
|
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ENST00000684126.1:n.933G>A
|
|
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ENST00000684688.1:n.1424G>A
|
|
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ENST00000204679.9:c.799G>A
MANE Select
|
ENSP00000204679.4:p.Gly267Ser
|
|
ENST00000204679.8:c.799G>A
|
ENSP00000204679.4:p.Gly267Ser
|
|
ENST00000527076.1:n.2022G>A
|
|
|
ENST00000527168.5:n.966G>A
|
|
|
ENST00000529957.5:n.898G>A
|
|
|
NM_032520.4:c.799G>A
|
NP_115909.1:p.Gly267Ser
|
|
XM_017023782.1:c.847G>A
|
XP_016879271.1:p.Gly283Ser
|
|
XM_017023783.1:c.439G>A
|
XP_016879272.1:p.Gly147Ser
|
|
NM_032520.5:c.799G>A
MANE Select
|
NP_115909.1:p.Gly267Ser
|
|