|
ENST00000340611.9:c.1428G>T
MANE Select
|
ENSP00000339637.4:p.Arg476Ser
|
|
|
ENST00000340611.8:c.1428G>T
|
ENSP00000339637.4:p.Arg476Ser
|
|
|
ENST00000467558.5:n.2800G>T
|
|
|
|
ENST00000469750.5:n.4000G>T
|
|
|
|
ENST00000473879.1:n.144G>T
|
|
|
|
ENST00000493232.5:n.4164G>T
|
|
|
|
NM_152743.3:c.1428G>T
|
NP_689956.2:p.Arg476Ser
|
|
|
XM_005249643.3:c.1428G>T
|
XP_005249700.1:p.Arg476Ser
|
|
|
XM_011515177.1:c.1512G>T
|
XP_011513479.1:p.Arg504Ser
|
|
|
XM_011515178.1:c.1512G>T
|
XP_011513480.1:p.Arg504Ser
|
|
|
XM_011515179.1:c.1509G>T
|
XP_011513481.1:p.Arg503Ser
|
|
|
XM_011515180.1:c.1482G>T
|
XP_011513482.1:p.Arg494Ser
|
|
|
XM_011515181.1:c.1512G>T
|
XP_011513483.1:p.Arg504Ser
|
|
|
XM_011515182.1:c.1512G>T
|
XP_011513484.1:p.Arg504Ser
|
|
|
XM_011515183.1:c.987G>T
|
XP_011513485.1:p.Arg329Ser
|
|
|
XM_011515184.1:c.987G>T
|
XP_011513486.1:p.Arg329Ser
|
|
|
XM_011515185.1:c.1428G>T
|
XP_011513487.1:p.Arg476Ser
|
|
|
XM_011515186.1:c.1512G>T
|
XP_011513488.1:p.Arg504Ser
|
|
|
XM_011515187.1:c.84G>T
|
XP_011513489.1:p.Arg28Ser
|
|
|
NM_001350626.1:c.1428G>T
|
NP_001337555.1:p.Arg476Ser
|
|
|
NM_001350627.1:c.903G>T
|
NP_001337556.1:p.Arg301Ser
|
|
|
NR_146879.1:n.1845G>T
|
|
|
|
XM_011515177.2:c.1512G>T
|
XP_011513479.1:p.Arg504Ser
|
|
|
XM_011515179.2:c.1509G>T
|
XP_011513481.1:p.Arg503Ser
|
|
|
XM_011515181.2:c.1512G>T
|
XP_011513483.1:p.Arg504Ser
|
|
|
XM_011515182.2:c.1512G>T
|
XP_011513484.1:p.Arg504Ser
|
|
|
XM_011515184.3:c.987G>T
|
XP_011513486.1:p.Arg329Ser
|
|
|
XM_011515186.2:c.1512G>T
|
XP_011513488.1:p.Arg504Ser
|
|
|
XM_017011833.1:c.1425G>T
|
XP_016867322.1:p.Arg475Ser
|
|
|
XM_017011834.1:c.1425G>T
|
XP_016867323.1:p.Arg475Ser
|
|
|
XM_017011836.2:c.1428G>T
|
XP_016867325.1:p.Arg476Ser
|
|
|
XM_024446682.1:c.84G>T
|
XP_024302450.1:p.Arg28Ser
|
|
|
NM_152743.4:c.1428G>T
MANE Select
|
NP_689956.2:p.Arg476Ser
|
|
|
NM_001350626.2:c.1428G>T
|
NP_001337555.1:p.Arg476Ser
|
|
|
NM_001350627.2:c.903G>T
|
NP_001337556.1:p.Arg301Ser
|
|
|
NR_146879.2:n.1611G>T
|
|
|
