ENST00000376020.9:c.490C>T
MANE Select
|
ENSP00000365188.2:p.Gln164Ter
|
|
ENST00000376020.8:c.490C>T
|
ENSP00000365188.2:p.Gln164Ter
|
|
ENST00000289292.11:c.490C>T
|
ENSP00000289292.7:p.Gln164Ter
|
|
ENST00000376020.6:c.490C>T
|
ENSP00000365188.2:p.Gln164Ter
|
|
ENST00000460112.3:c.142C>T
|
ENSP00000421450.1:p.Gln48Ter
|
|
NM_020717.3:c.490C>T
|
NP_065768.2:p.Gln164Ter
|
|
NR_027121.1:n.516C>T
|
|
|
XM_006724590.2:c.142C>T
|
XP_006724653.1:p.Gln48Ter
|
|
XM_006724591.2:c.16C>T
|
XP_006724654.1:p.Gln6Ter
|
|
XM_011530800.1:c.355C>T
|
XP_011529102.1:p.Gln119Ter
|
|
XM_011530801.1:c.490C>T
|
XP_011529103.1:p.Gln164Ter
|
|
XR_938367.1:n.608C>T
|
|
|
XR_938368.1:n.608C>T
|
|
|
XM_017029682.2:c.490C>T
|
XP_016885171.1:p.Gln164Ter
|
|
XM_017029683.1:c.355C>T
|
XP_016885172.1:p.Gln119Ter
|
|
XM_017029684.1:c.142C>T
|
XP_016885173.1:p.Gln48Ter
|
|
XM_017029685.2:c.490C>T
|
XP_016885174.1:p.Gln164Ter
|
|
XM_017029686.1:c.16C>T
|
XP_016885175.1:p.Gln6Ter
|
|
XM_017029687.2:c.490C>T
|
XP_016885176.1:p.Gln164Ter
|
|
XR_001755716.2:n.621C>T
|
|
|
XR_001755717.2:n.621C>T
|
|
|
XR_001755718.2:n.621C>T
|
|
|
NM_020717.5:c.490C>T
MANE Select
|
NP_065768.2:p.Gln164Ter
|
|
NR_027121.3:n.666C>T
|
|
|
NR_172068.1:n.531C>T
|
|
|
NR_172069.1:n.586C>T
|
|
|
NR_172070.1:n.451C>T
|
|
|