ENST00000254108.12:c.201A>T
MANE Select
|
ENSP00000254108.8:p.Gly67=
|
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ENST00000254108.11:c.201A>T
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ENSP00000254108.7:p.Gly67=
|
|
ENST00000380244.7:c.198A>T
|
ENSP00000369594.3:p.Gly66=
|
|
ENST00000487509.6:n.266A>T
|
|
|
ENST00000487974.1:n.319A>T
|
|
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ENST00000566605.5:c.201A>T
|
ENSP00000455073.1:p.Gly67=
|
|
ENST00000568685.1:c.201A>T
|
ENSP00000455282.1:p.Gly67=
|
|
NM_001170634.1:c.198A>T
|
NP_001164105.1:p.Gly66=
|
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NM_001170937.1:c.201A>T
|
NP_001164408.1:p.Gly67=
|
|
NM_004960.3:c.201A>T , LRG_655t1:c.201A>T
|
NP_004951.1:p.Gly67=
|
|
NR_028388.2:n.306A>T
|
|
|
XM_005255233.3:c.-380A>T
|
XP_005255290.1:n.-380A>T
|
|
XM_011545781.1:c.201A>T
|
XP_011544083.1:p.Gly67=
|
|
XM_005255233.5:c.-380A>T
|
XP_005255290.1:n.-380A>T
|
|
XM_024450221.1:c.198A>T
|
XP_024305989.1:p.Gly66=
|
|
NM_004960.4:c.201A>T
MANE Select
|
NP_004951.1:p.Gly67=
|
|