ENST00000389048.8:c.3564A>T
MANE Select
|
ENSP00000373700.3:p.Gln1188His
|
|
ENST00000431873.6:c.791A>T
|
|
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ENST00000638605.1:n.441A>T
|
|
|
ENST00000642122.1:c.360A>T
|
ENSP00000493203.1:p.Gln120His
|
|
ENST00000389048.7:c.3564A>T
|
ENSP00000373700.3:p.Gln1188His
|
|
ENST00000431873.5:c.444A>T
|
ENSP00000414027.2:p.Gln148His
|
|
ENST00000618119.4:c.2433A>T
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ENSP00000482733.1:p.Gln811His
|
|
NM_004304.4:c.3564A>T
|
NP_004295.2:p.Gln1188His
|
|
NM_001353765.1:c.360A>T
|
NP_001340694.1:p.Gln120His
|
|
XM_024452778.1:c.717A>T
|
XP_024308546.1:p.Gln239His
|
|
XM_024452779.1:c.360A>T
|
XP_024308547.1:p.Gln120His
|
|
NM_004304.5:c.3564A>T
MANE Select
|
NP_004295.2:p.Gln1188His
|
|
NM_001353765.2:c.360A>T
|
NP_001340694.1:p.Gln120His
|
|