ENST00000399408.7:c.4047C>A
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ENSP00000382340.4:p.Gly1349=
|
|
ENST00000399410.8:c.4017C>A
MANE Select
|
ENSP00000382342.3:p.Gly1339=
|
|
ENST00000572882.3:c.3840C>A
|
ENSP00000461615.2:p.Gly1280=
|
|
ENST00000676806.1:n.743C>A
|
|
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ENST00000677164.1:c.3546C>A
|
ENSP00000502873.1:p.Gly1182=
|
|
ENST00000678422.1:c.*1309C>A
|
ENSP00000503954.1:n.*1309C>A
|
|
ENST00000399408.6:c.3069C>A
|
ENSP00000382340.3:p.Gly1023=
|
|
ENST00000399410.7:c.4017C>A
|
ENSP00000382342.3:p.Gly1339=
|
|
ENST00000572882.2:c.3742C>A
|
|
|
NM_004996.3:c.4017C>A
|
NP_004987.2:p.Gly1339=
|
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XM_011522497.1:c.3993C>A
|
XP_011520799.1:p.Gly1331=
|
|
XM_011522498.1:c.3924C>A
|
XP_011520800.1:p.Gly1308=
|
|
XM_011522498.2:c.3924C>A
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XP_011520800.1:p.Gly1308=
|
|
XM_017023237.1:c.4071C>A
|
XP_016878726.1:p.Gly1357=
|
|
XM_017023238.1:c.3945C>A
|
XP_016878727.1:p.Gly1315=
|
|
XM_017023239.1:c.3933C>A
|
XP_016878728.1:p.Gly1311=
|
|
XM_017023240.1:c.3894C>A
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XP_016878729.1:p.Gly1298=
|
|
XM_017023241.1:c.3807C>A
|
XP_016878730.1:p.Gly1269=
|
|
XM_017023242.1:c.3726C>A
|
XP_016878731.1:p.Gly1242=
|
|
NM_004996.4:c.4017C>A
MANE Select
|
NP_004987.2:p.Gly1339=
|
|