ENST00000233575.7:c.808G=
MANE Select
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ENSP00000233575.2:p.Gly270=
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ENST00000233575.6:c.808G=
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ENSP00000233575.2:p.Gly270=
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|
ENST00000427123.5:c.*618G=
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ENSP00000405399.1:n.*618G=
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ENST00000440760.5:c.*653G=
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ENSP00000399727.1:n.*653G=
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ENST00000453453.1:c.*335G=
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ENSP00000401922.1:n.*335G=
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ENST00000493711.1:n.525G=
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|
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ENST00000537606.5:c.733G=
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ENSP00000439208.1:p.Gly245=
|
|
NM_001267059.1:c.772G=
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NP_001253988.1:p.Gly258=
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NM_001267060.1:c.733G=
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NP_001253989.1:p.Gly245=
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|
NM_001267061.1:c.748G=
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NP_001253990.1:p.Gly250=
|
|
NM_014748.3:c.808G=
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NP_055563.1:p.Gly270=
|
|
NR_049782.1:n.1181G=
|
|
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NR_049783.1:n.1154G=
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|
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NR_049784.1:n.1130G=
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|
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NR_049785.1:n.1063G=
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|
|
NR_049786.1:n.1012G=
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|
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NR_049787.1:n.863G=
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|
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NR_049788.1:n.793G=
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|
|
XM_011533203.1:c.166G=
|
XP_011531505.1:p.Gly56=
|
|
XM_011533203.2:c.166G=
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XP_011531505.1:p.Gly56=
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|
XM_017005405.2:c.166G=
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XP_016860894.1:p.Gly56=
|
|
NM_014748.4:c.808G=
MANE Select
|
NP_055563.1:p.Gly270=
|
|
NM_001267059.2:c.772G=
|
NP_001253988.1:p.Gly258=
|
|
NM_001267061.2:c.748G=
|
NP_001253990.1:p.Gly250=
|
|
NR_049782.2:n.1061G=
|
|
|
NR_049783.2:n.1034G=
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|
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NR_049784.2:n.1010G=
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|
|
NR_049785.2:n.943G=
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|
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NR_049786.2:n.892G=
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|
|
NR_049787.2:n.743G=
|
|
|
NR_049788.2:n.673G=
|
|
|
NM_001267060.2:c.733G=
|
NP_001253989.1:p.Gly245=
|
|