ENST00000699510.1:c.346C=
|
ENSP00000514405.1:p.His116=
|
|
ENST00000699511.1:c.588C=
|
|
|
ENST00000207549.9:c.1411C=
MANE Select
|
ENSP00000207549.3:p.His471=
|
|
ENST00000207549.8:c.1411C=
|
ENSP00000207549.3:p.His471=
|
|
ENST00000412096.6:c.1411C=
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ENSP00000388093.1:p.His471=
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ENST00000586147.1:c.139C=
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ENSP00000466543.1:p.His47=
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ENST00000587105.1:c.530C=
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|
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ENST00000591563.5:n.1681C=
|
|
|
NM_199242.2:c.1411C= , LRG_122t1:c.1411C=
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NP_954712.1:p.His471=
|
|
XM_011524504.1:c.1411C=
|
XP_011522806.1:p.His471=
|
|
XM_011524505.1:c.1411C=
|
XP_011522807.1:p.His471=
|
|
XM_011524506.1:c.1408C=
|
XP_011522808.1:p.His470=
|
|
XM_011524507.1:c.802C=
|
XP_011522809.1:p.His268=
|
|
XM_011524508.1:c.802C=
|
XP_011522810.1:p.His268=
|
|
XM_011524504.2:c.1411C=
|
XP_011522806.1:p.His471=
|
|
XM_011524507.2:c.802C=
|
XP_011522809.1:p.His268=
|
|
XM_024450640.1:c.802C=
|
XP_024306408.1:p.His268=
|
|
NM_199242.3:c.1411C=
MANE Select
|
NP_954712.1:p.His471=
|
|