ENST00000233575.7:c.702T>G
MANE Select
|
ENSP00000233575.2:p.Arg234=
|
|
ENST00000233575.6:c.702T>G
|
ENSP00000233575.2:p.Arg234=
|
|
ENST00000427123.5:c.*512T>G
|
ENSP00000405399.1:n.*512T>G
|
|
ENST00000440760.5:c.*547T>G
|
ENSP00000399727.1:n.*547T>G
|
|
ENST00000453453.1:c.*229T>G
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ENSP00000401922.1:n.*229T>G
|
|
ENST00000493711.1:n.419T>G
|
|
|
ENST00000494893.5:n.878T>G
|
|
|
ENST00000537606.5:c.627T>G
|
ENSP00000439208.1:p.Arg209=
|
|
NM_001267059.1:c.666T>G
|
NP_001253988.1:p.Arg222=
|
|
NM_001267060.1:c.627T>G
|
NP_001253989.1:p.Arg209=
|
|
NM_001267061.1:c.642T>G
|
NP_001253990.1:p.Arg214=
|
|
NM_014748.3:c.702T>G
|
NP_055563.1:p.Arg234=
|
|
NR_049782.1:n.1075T>G
|
|
|
NR_049783.1:n.1048T>G
|
|
|
NR_049784.1:n.1024T>G
|
|
|
NR_049785.1:n.957T>G
|
|
|
NR_049786.1:n.906T>G
|
|
|
NR_049787.1:n.757T>G
|
|
|
NR_049788.1:n.687T>G
|
|
|
XM_011533203.1:c.60T>G
|
XP_011531505.1:p.Arg20=
|
|
XM_011533203.2:c.60T>G
|
XP_011531505.1:p.Arg20=
|
|
XM_017005405.2:c.60T>G
|
XP_016860894.1:p.Arg20=
|
|
NM_014748.4:c.702T>G
MANE Select
|
NP_055563.1:p.Arg234=
|
|
NM_001267059.2:c.666T>G
|
NP_001253988.1:p.Arg222=
|
|
NM_001267061.2:c.642T>G
|
NP_001253990.1:p.Arg214=
|
|
NR_049782.2:n.955T>G
|
|
|
NR_049783.2:n.928T>G
|
|
|
NR_049784.2:n.904T>G
|
|
|
NR_049785.2:n.837T>G
|
|
|
NR_049786.2:n.786T>G
|
|
|
NR_049787.2:n.637T>G
|
|
|
NR_049788.2:n.567T>G
|
|
|
NM_001267060.2:c.627T>G
|
NP_001253989.1:p.Arg209=
|
|