ENST00000303115.8:c.572T>G
MANE Select
|
ENSP00000306157.3:p.Leu191Arg
|
|
ENST00000303115.7:c.572T>G
|
ENSP00000306157.3:p.Leu191Arg
|
|
ENST00000506850.5:c.572T>G
|
ENSP00000421207.1:p.Leu191Arg
|
|
ENST00000509668.1:n.314T>G
|
|
|
ENST00000514217.5:c.538-1998T>G
|
ENSP00000427688.1:n.538-1998T>G
|
|
NM_002185.3:c.572T>G
|
NP_002176.2:p.Leu191Arg
|
|
NR_120485.1:n.641-1998T>G
|
|
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XM_005248299.2:c.572T>G
|
XP_005248356.1:p.Leu191Arg
|
|
XM_005248300.1:c.572T>G
|
XP_005248357.1:p.Leu191Arg
|
|
XM_011514037.1:c.572T>G
|
XP_011512339.1:p.Leu191Arg
|
|
NM_002185.4:c.572T>G
|
NP_002176.2:p.Leu191Arg
|
|
NR_120485.2:n.667-1998T>G
|
|
|
XM_005248299.4:c.572T>G
|
XP_005248356.1:p.Leu191Arg
|
|
NM_002185.5:c.572T>G
MANE Select
|
NP_002176.2:p.Leu191Arg
|
|
NR_120485.3:n.625-1998T>G
|
|
|