|
ENST00000340611.9:c.1457G>T
MANE Select
|
ENSP00000339637.4:p.Gly486Val
|
|
|
ENST00000340611.8:c.1457G>T
|
ENSP00000339637.4:p.Gly486Val
|
|
|
ENST00000467558.5:n.2829G>T
|
|
|
|
ENST00000469750.5:n.4029G>T
|
|
|
|
ENST00000473879.1:n.173G>T
|
|
|
|
ENST00000493232.5:n.4193G>T
|
|
|
|
NM_152743.3:c.1457G>T
|
NP_689956.2:p.Gly486Val
|
|
|
XM_005249643.3:c.1457G>T
|
XP_005249700.1:p.Gly486Val
|
|
|
XM_011515177.1:c.1541G>T
|
XP_011513479.1:p.Gly514Val
|
|
|
XM_011515178.1:c.1541G>T
|
XP_011513480.1:p.Gly514Val
|
|
|
XM_011515179.1:c.1538G>T
|
XP_011513481.1:p.Gly513Val
|
|
|
XM_011515180.1:c.1511G>T
|
XP_011513482.1:p.Gly504Val
|
|
|
XM_011515181.1:c.1541G>T
|
XP_011513483.1:p.Gly514Val
|
|
|
XM_011515182.1:c.1541G>T
|
XP_011513484.1:p.Gly514Val
|
|
|
XM_011515183.1:c.1016G>T
|
XP_011513485.1:p.Gly339Val
|
|
|
XM_011515184.1:c.1016G>T
|
XP_011513486.1:p.Gly339Val
|
|
|
XM_011515185.1:c.1457G>T
|
XP_011513487.1:p.Gly486Val
|
|
|
XM_011515186.1:c.1541G>T
|
XP_011513488.1:p.Gly514Val
|
|
|
XM_011515187.1:c.113G>T
|
XP_011513489.1:p.Gly38Val
|
|
|
NM_001350626.1:c.1457G>T
|
NP_001337555.1:p.Gly486Val
|
|
|
NM_001350627.1:c.932G>T
|
NP_001337556.1:p.Gly311Val
|
|
|
NR_146879.1:n.1874G>T
|
|
|
|
XM_011515177.2:c.1541G>T
|
XP_011513479.1:p.Gly514Val
|
|
|
XM_011515179.2:c.1538G>T
|
XP_011513481.1:p.Gly513Val
|
|
|
XM_011515181.2:c.1541G>T
|
XP_011513483.1:p.Gly514Val
|
|
|
XM_011515182.2:c.1541G>T
|
XP_011513484.1:p.Gly514Val
|
|
|
XM_011515184.3:c.1016G>T
|
XP_011513486.1:p.Gly339Val
|
|
|
XM_011515186.2:c.1541G>T
|
XP_011513488.1:p.Gly514Val
|
|
|
XM_017011833.1:c.1454G>T
|
XP_016867322.1:p.Gly485Val
|
|
|
XM_017011834.1:c.1454G>T
|
XP_016867323.1:p.Gly485Val
|
|
|
XM_017011836.2:c.1457G>T
|
XP_016867325.1:p.Gly486Val
|
|
|
XM_024446682.1:c.113G>T
|
XP_024302450.1:p.Gly38Val
|
|
|
NM_152743.4:c.1457G>T
MANE Select
|
NP_689956.2:p.Gly486Val
|
|
|
NM_001350626.2:c.1457G>T
|
NP_001337555.1:p.Gly486Val
|
|
|
NM_001350627.2:c.932G>T
|
NP_001337556.1:p.Gly311Val
|
|
|
NR_146879.2:n.1640G>T
|
|
|
