ENST00000456935.7:c.439C>T
MANE Select
|
ENSP00000395473.2:p.Arg147Cys
|
|
ENST00000221363.8:c.439C>T
|
ENSP00000221363.4:p.Arg147Cys
|
|
ENST00000456935.6:c.439C>T
|
ENSP00000395473.2:p.Arg147Cys
|
|
ENST00000466794.5:n.421C>T
|
|
|
ENST00000486847.2:c.333+369C>T
|
ENSP00000470174.1:n.333+369C>T
|
|
ENST00000596512.5:n.377C>T
|
|
|
ENST00000597961.1:c.430C>T
|
ENSP00000472710.1:p.Arg144Cys
|
|
ENST00000598876.1:c.466C>T
|
ENSP00000470533.1:p.Arg156Cys
|
|
NM_000528.3:c.439C>T
|
NP_000519.2:p.Arg147Cys
|
|
NM_001173498.1:c.439C>T
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NP_001166969.1:p.Arg147Cys
|
|
XM_005259913.1:c.439C>T
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XP_005259970.1:p.Arg147Cys
|
|
XM_005259913.2:c.439C>T
|
XP_005259970.1:p.Arg147Cys
|
|
XM_024451518.1:c.-580C>T
|
XP_024307286.1:n.-580C>T
|
|
NM_000528.4:c.439C>T
MANE Select
|
NP_000519.2:p.Arg147Cys
|
|
NM_001173498.2:c.439C>T
|
NP_001166969.1:p.Arg147Cys
|
|