ENST00000233575.7:c.756G>T
MANE Select
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ENSP00000233575.2:p.Glu252Asp
|
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ENST00000233575.6:c.756G>T
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ENSP00000233575.2:p.Glu252Asp
|
|
ENST00000427123.5:c.*566G>T
|
ENSP00000405399.1:n.*566G>T
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ENST00000440760.5:c.*601G>T
|
ENSP00000399727.1:n.*601G>T
|
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ENST00000453453.1:c.*283G>T
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ENSP00000401922.1:n.*283G>T
|
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ENST00000493711.1:n.473G>T
|
|
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ENST00000494893.5:n.932G>T
|
|
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ENST00000537606.5:c.681G>T
|
ENSP00000439208.1:p.Glu227Asp
|
|
NM_001267059.1:c.720G>T
|
NP_001253988.1:p.Glu240Asp
|
|
NM_001267060.1:c.681G>T
|
NP_001253989.1:p.Glu227Asp
|
|
NM_001267061.1:c.696G>T
|
NP_001253990.1:p.Glu232Asp
|
|
NM_014748.3:c.756G>T
|
NP_055563.1:p.Glu252Asp
|
|
NR_049782.1:n.1129G>T
|
|
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NR_049783.1:n.1102G>T
|
|
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NR_049784.1:n.1078G>T
|
|
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NR_049785.1:n.1011G>T
|
|
|
NR_049786.1:n.960G>T
|
|
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NR_049787.1:n.811G>T
|
|
|
NR_049788.1:n.741G>T
|
|
|
XM_011533203.1:c.114G>T
|
XP_011531505.1:p.Glu38Asp
|
|
XM_011533203.2:c.114G>T
|
XP_011531505.1:p.Glu38Asp
|
|
XM_017005405.2:c.114G>T
|
XP_016860894.1:p.Glu38Asp
|
|
NM_014748.4:c.756G>T
MANE Select
|
NP_055563.1:p.Glu252Asp
|
|
NM_001267059.2:c.720G>T
|
NP_001253988.1:p.Glu240Asp
|
|
NM_001267061.2:c.696G>T
|
NP_001253990.1:p.Glu232Asp
|
|
NR_049782.2:n.1009G>T
|
|
|
NR_049783.2:n.982G>T
|
|
|
NR_049784.2:n.958G>T
|
|
|
NR_049785.2:n.891G>T
|
|
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NR_049786.2:n.840G>T
|
|
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NR_049787.2:n.691G>T
|
|
|
NR_049788.2:n.621G>T
|
|
|
NM_001267060.2:c.681G>T
|
NP_001253989.1:p.Glu227Asp
|
|