ENST00000334888.10:c.146T>G
|
ENSP00000334844.5:p.Leu49Arg
|
|
ENST00000544795.6:n.423T>G
|
|
|
ENST00000684926.1:n.162T>G
|
|
|
ENST00000688959.1:c.-114T>G
|
ENSP00000509213.1:n.-114T>G
|
|
ENST00000690736.1:c.146T>G
|
ENSP00000508542.1:p.Leu49Arg
|
|
ENST00000515837.7:c.146T>G
MANE Select
|
ENSP00000440638.1:p.Leu49Arg
|
|
ENST00000334888.9:c.146T>G
|
ENSP00000334844.5:p.Leu49Arg
|
|
ENST00000398979.7:c.-38T>G
|
ENSP00000381950.3:n.-38T>G
|
|
ENST00000515837.6:c.146T>G
|
ENSP00000440638.1:p.Leu49Arg
|
|
ENST00000541473.1:n.160T>G
|
|
|
ENST00000544795.5:n.162T>G
|
|
|
NM_001173990.2:c.146T>G
|
NP_001167461.1:p.Leu49Arg
|
|
NM_001173991.2:c.146T>G
|
NP_001167462.1:p.Leu49Arg
|
|
NM_016499.5:c.-38T>G
|
NP_057583.2:n.-38T>G
|
|
XM_005274039.3:c.-38T>G
|
XP_005274096.1:n.-38T>G
|
|
NM_001330285.1:c.-38T>G
|
NP_001317214.1:n.-38T>G
|
|
XM_005274039.4:c.-38T>G
|
XP_005274096.1:n.-38T>G
|
|
NM_001173990.3:c.146T>G
MANE Select
|
NP_001167461.1:p.Leu49Arg
|
|
NM_001173991.3:c.146T>G
|
NP_001167462.1:p.Leu49Arg
|
|
NM_001330285.2:c.-38T>G
|
NP_001317214.1:n.-38T>G
|
|
NM_016499.6:c.-38T>G
|
NP_057583.2:n.-38T>G
|
|