ENST00000479013.7:c.25G>A
|
ENSP00000417990.3:p.Gly9Arg
|
|
ENST00000487418.8:c.25G>A
MANE Select
|
ENSP00000418397.3:p.Gly9Arg
|
|
ENST00000610693.5:c.25G>A
|
ENSP00000479359.2:p.Gly9Arg
|
|
ENST00000650656.1:c.34G>A
|
ENSP00000498731.1:p.Gly12Arg
|
|
ENST00000651168.1:c.34G>A
|
ENSP00000499074.1:p.Gly12Arg
|
|
ENST00000479013.6:c.34G>A
|
ENSP00000417990.2:p.Gly12Arg
|
|
ENST00000487418.6:c.34G>A
|
ENSP00000418397.2:p.Gly12Arg
|
|
ENST00000610693.4:c.34G>A
|
ENSP00000479359.1:p.Gly12Arg
|
|
NM_001159508.1:c.34G>A
|
NP_001152980.1:p.Gly12Arg
|
|
NM_002225.3:c.34G>A
|
NP_002216.2:p.Gly12Arg
|
|
XM_005254350.2:c.34G>A
|
XP_005254407.1:p.Gly12Arg
|
|
XM_005254356.2:c.34G>A
|
XP_005254413.1:p.Gly12Arg
|
|
XM_006720492.2:c.34G>A
|
XP_006720555.1:p.Gly12Arg
|
|
XM_006720493.2:c.34G>A
|
XP_006720556.1:p.Gly12Arg
|
|
XM_006720494.2:c.34G>A
|
XP_006720557.1:p.Gly12Arg
|
|
XM_006720495.2:c.34G>A
|
XP_006720558.1:p.Gly12Arg
|
|
XM_011521523.1:c.34G>A
|
XP_011519825.1:p.Gly12Arg
|
|
XM_011521524.1:c.34G>A
|
XP_011519826.1:p.Gly12Arg
|
|
XR_243097.3:n.34G>A
|
|
|
XR_243098.2:n.34G>A
|
|
|
XR_429453.2:n.135G>A
|
|
|
NM_001159508.2:c.25G>A
|
NP_001152980.2:p.Gly9Arg
|
|
NM_001354597.2:c.-403G>A
|
NP_001341526.1:n.-403G>A
|
|
NM_001354598.2:c.25G>A
|
NP_001341527.2:p.Gly9Arg
|
|
NM_001354599.2:c.25G>A
|
NP_001341528.2:p.Gly9Arg
|
|
NM_001354600.2:c.25G>A
|
NP_001341529.2:p.Gly9Arg
|
|
NM_001354601.2:c.25G>A
|
NP_001341530.2:p.Gly9Arg
|
|
NM_002225.4:c.25G>A
|
NP_002216.3:p.Gly9Arg
|
|
NR_148925.1:n.56G>A
|
|
|
XM_006720495.3:c.34G>A
|
XP_006720558.1:p.Gly12Arg
|
|
XM_017022149.1:c.34G>A
|
XP_016877638.1:p.Gly12Arg
|
|
XM_017022150.1:c.34G>A
|
XP_016877639.1:p.Gly12Arg
|
|
XM_017022153.1:c.34G>A
|
XP_016877642.1:p.Gly12Arg
|
|
XM_017022155.2:c.34G>A
|
XP_016877644.1:p.Gly12Arg
|
|
XM_017022157.1:c.34G>A
|
XP_016877646.1:p.Gly12Arg
|
|
XM_017022158.2:c.34G>A
|
XP_016877647.1:p.Gly12Arg
|
|
XR_001751263.1:n.5G>A
|
|
|
XR_001751264.1:n.46G>A
|
|
|
NM_001159508.3:c.25G>A
|
NP_001152980.2:p.Gly9Arg
|
|
NM_001354597.3:c.-403G>A
|
NP_001341526.1:n.-403G>A
|
|
NM_001354598.3:c.25G>A
|
NP_001341527.2:p.Gly9Arg
|
|
NM_001354599.3:c.25G>A
|
NP_001341528.2:p.Gly9Arg
|
|
NM_001354600.3:c.25G>A
|
NP_001341529.2:p.Gly9Arg
|
|
NM_001354601.3:c.25G>A
|
NP_001341530.2:p.Gly9Arg
|
|
NM_002225.5:c.25G>A
MANE Select
|
NP_002216.3:p.Gly9Arg
|
|
NR_148925.2:n.58G>A
|
|
|