ENST00000651671.1:c.6390G>C
MANE Select
|
ENSP00000498587.1:p.Gly2130=
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ENST00000679595.1:c.*1430G>C
|
ENSP00000506241.1:n.*1430G>C
|
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ENST00000679969.1:n.2986G>C
|
|
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ENST00000680003.1:n.2722G>C
|
|
|
ENST00000680133.1:c.6276G>C
|
ENSP00000505319.1:p.Gly2092=
|
|
ENST00000680218.1:c.6270G>C
|
ENSP00000505339.1:p.Gly2090=
|
|
ENST00000680668.1:c.6276G>C
|
ENSP00000506336.1:p.Gly2092=
|
|
ENST00000680778.1:c.3987G>C
|
ENSP00000506033.1:p.Gly1329=
|
|
ENST00000680924.1:c.*3790G>C
|
ENSP00000506031.1:n.*3790G>C
|
|
ENST00000681135.1:c.*3999G>C
|
ENSP00000506636.1:n.*3999G>C
|
|
ENST00000681298.1:n.4495G>C
|
|
|
ENST00000681454.1:c.*5626G>C
|
ENSP00000505763.1:n.*5626G>C
|
|
ENST00000277541.6:c.6390G>C
|
ENSP00000277541.6:p.Gly2130=
|
|
NM_017617.3:c.6390G>C
|
NP_060087.3:p.Gly2130=
|
|
XM_011518717.1:c.5691G>C
|
XP_011517019.1:p.Gly1897=
|
|
NM_017617.5:c.6390G>C
MANE Select
|
NP_060087.3:p.Gly2130=
|
|
XM_011518717.2:c.5667G>C
|
XP_011517019.2:p.Gly1889=
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