ENST00000367400.8:c.3173A>T
MANE Select
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ENSP00000356370.3:p.Glu1058Val
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ENST00000638467.1:c.3173A>T
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ENSP00000491102.1:p.Glu1058Val
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ENST00000681519.1:c.2054A>T
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ENSP00000505267.1:p.Glu685Val
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ENST00000367397.1:c.1316A>T
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ENSP00000356367.1:p.Glu439Val
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ENST00000367399.6:c.2837A>T
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ENSP00000356369.2:p.Glu946Val
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ENST00000367400.7:c.3173A>T
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ENSP00000356370.3:p.Glu1058Val
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ENST00000484075.5:c.3173A>T
|
ENSP00000433932.1:p.Glu1058Val
|
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ENST00000535699.5:c.3101A>T
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ENSP00000438786.1:p.Glu1034Val
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ENST00000538660.5:c.2129-564A>T
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ENSP00000438091.1:n.2129-564A>T
|
|
NM_001193640.1:c.2837A>T
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NP_001180569.1:p.Glu946Val
|
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NM_001257965.1:c.3101A>T
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NP_001244894.1:p.Glu1034Val
|
|
NM_001257966.1:c.2129-564A>T
|
NP_001244895.1:n.2129-564A>T
|
|
NM_201253.2:c.3173A>T
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NP_957705.1:p.Glu1058Val
|
|
NR_047563.1:n.3174A>T
|
|
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NR_047564.1:n.3382A>T
|
|
|
XM_011509365.1:c.3173A>T
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XP_011507667.1:p.Glu1058Val
|
|
XM_011509366.1:c.3173A>T
|
XP_011507668.1:p.Glu1058Val
|
|
XM_011509367.1:c.3173A>T
|
XP_011507669.1:p.Glu1058Val
|
|
XM_011509368.1:c.2591A>T
|
XP_011507670.1:p.Glu864Val
|
|
XM_011509369.1:c.1616A>T
|
XP_011507671.1:p.Glu539Val
|
|
XM_011509365.2:c.3173A>T
|
XP_011507667.1:p.Glu1058Val
|
|
XM_011509369.2:c.1616A>T
|
XP_011507671.1:p.Glu539Val
|
|
XM_017000851.1:c.2330A>T
|
XP_016856340.1:p.Glu777Val
|
|
XM_017000852.1:c.3308A>T
|
XP_016856341.1:p.Glu1103Val
|
|
NM_201253.3:c.3173A>T
MANE Select
|
NP_957705.1:p.Glu1058Val
|
|
NM_001193640.2:c.2837A>T
|
NP_001180569.1:p.Glu946Val
|
|
NM_001257965.2:c.3101A>T
|
NP_001244894.1:p.Glu1034Val
|
|
NR_047563.2:n.3126A>T
|
|
|
NR_047564.2:n.3334A>T
|
|
|
NM_001257966.2:c.2129-564A>T
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NP_001244895.1:n.2129-564A>T
|
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