ENST00000233575.7:c.798G>A
MANE Select
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ENSP00000233575.2:p.Leu266=
|
|
ENST00000233575.6:c.798G>A
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ENSP00000233575.2:p.Leu266=
|
|
ENST00000427123.5:c.*608G>A
|
ENSP00000405399.1:n.*608G>A
|
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ENST00000440760.5:c.*643G>A
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ENSP00000399727.1:n.*643G>A
|
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ENST00000453453.1:c.*325G>A
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ENSP00000401922.1:n.*325G>A
|
|
ENST00000493711.1:n.515G>A
|
|
|
ENST00000537606.5:c.723G>A
|
ENSP00000439208.1:p.Leu241=
|
|
NM_001267059.1:c.762G>A
|
NP_001253988.1:p.Leu254=
|
|
NM_001267060.1:c.723G>A
|
NP_001253989.1:p.Leu241=
|
|
NM_001267061.1:c.738G>A
|
NP_001253990.1:p.Leu246=
|
|
NM_014748.3:c.798G>A
|
NP_055563.1:p.Leu266=
|
|
NR_049782.1:n.1171G>A
|
|
|
NR_049783.1:n.1144G>A
|
|
|
NR_049784.1:n.1120G>A
|
|
|
NR_049785.1:n.1053G>A
|
|
|
NR_049786.1:n.1002G>A
|
|
|
NR_049787.1:n.853G>A
|
|
|
NR_049788.1:n.783G>A
|
|
|
XM_011533203.1:c.156G>A
|
XP_011531505.1:p.Leu52=
|
|
XM_011533203.2:c.156G>A
|
XP_011531505.1:p.Leu52=
|
|
XM_017005405.2:c.156G>A
|
XP_016860894.1:p.Leu52=
|
|
NM_014748.4:c.798G>A
MANE Select
|
NP_055563.1:p.Leu266=
|
|
NM_001267059.2:c.762G>A
|
NP_001253988.1:p.Leu254=
|
|
NM_001267061.2:c.738G>A
|
NP_001253990.1:p.Leu246=
|
|
NR_049782.2:n.1051G>A
|
|
|
NR_049783.2:n.1024G>A
|
|
|
NR_049784.2:n.1000G>A
|
|
|
NR_049785.2:n.933G>A
|
|
|
NR_049786.2:n.882G>A
|
|
|
NR_049787.2:n.733G>A
|
|
|
NR_049788.2:n.663G>A
|
|
|
NM_001267060.2:c.723G>A
|
NP_001253989.1:p.Leu241=
|
|