ENST00000368802.8:c.9155G>T
(REV3L)
MANE Select
|
ENSP00000357792.3:p.Gly3052Val
|
|
ENST00000666581.2:n.277+29300C>A
(MFSD4B)
|
|
|
ENST00000673245.1:n.273+11683C>A
(MFSD4B)
|
|
|
ENST00000673446.1:n.179+39621C>A
(MFSD4B)
|
|
|
ENST00000358835.7:c.9155G>T
(REV3L)
|
ENSP00000351697.3:p.Gly3052Val
|
|
ENST00000368802.7:c.9155G>T
(REV3L)
|
ENSP00000357792.3:p.Gly3052Val
|
|
ENST00000368805.5:c.9155G>T
(REV3L)
|
ENSP00000357795.1:p.Gly3052Val
|
|
ENST00000422377.5:c.*9139G>T
(REV3L)
|
ENSP00000393184.1:n.*9139G>T
|
|
ENST00000434009.5:c.*9246G>T
(REV3L)
|
ENSP00000391605.1:n.*9246G>T
|
|
ENST00000435970.5:c.8921G>T
(REV3L)
|
ENSP00000402003.1:p.Gly2974Val
|
|
ENST00000462119.5:n.1292G>T
(REV3L)
|
|
|
NM_001286431.1:c.8921G>T
(REV3L)
|
NP_001273360.1:p.Gly2974Val
|
|
NM_001286432.1:c.8921G>T
(REV3L)
|
NP_001273361.1:p.Gly2974Val
|
|
NM_002912.4:c.9155G>T
(REV3L)
|
NP_002903.3:p.Gly3052Val
|
|
XM_006715543.2:c.9155G>T
(REV3L)
|
XP_006715606.1:p.Gly3052Val
|
|
XM_006715544.2:c.8921G>T
(REV3L)
|
XP_006715607.1:p.Gly2974Val
|
|
XM_011536028.1:c.9236G>T
(REV3L)
|
XP_011534330.1:p.Gly3079Val
|
|
XM_011536029.1:c.9233G>T
(REV3L)
|
XP_011534331.1:p.Gly3078Val
|
|
XM_011536030.1:c.9158G>T
(REV3L)
|
XP_011534332.1:p.Gly3053Val
|
|
XM_011536031.1:c.9002G>T
(REV3L)
|
XP_011534333.1:p.Gly3001Val
|
|
XM_011536032.1:c.9002G>T
(REV3L)
|
XP_011534334.1:p.Gly3001Val
|
|
XR_942871.1:n.2045+29300C>A
|
|
|
XM_011536028.2:c.9236G>T
(REV3L)
|
XP_011534330.1:p.Gly3079Val
|
|
XM_011536029.3:c.9233G>T
(REV3L)
|
XP_011534331.1:p.Gly3078Val
|
|
XM_011536030.3:c.9158G>T
(REV3L)
|
XP_011534332.1:p.Gly3053Val
|
|
XM_011536031.3:c.9002G>T
(REV3L)
|
XP_011534333.1:p.Gly3001Val
|
|
XM_011536032.2:c.9002G>T
(REV3L)
|
XP_011534334.1:p.Gly3001Val
|
|
XM_017011152.2:c.8999G>T
(REV3L)
|
XP_016866641.1:p.Gly3000Val
|
|
XM_017011153.1:c.8999G>T
(REV3L)
|
XP_016866642.1:p.Gly3000Val
|
|
XM_017011154.1:c.8999G>T
(REV3L)
|
XP_016866643.1:p.Gly3000Val
|
|
XR_001743550.2:n.9341G>T
(REV3L)
|
|
|
XR_001743552.2:n.9263G>T
(REV3L)
|
|
|
XR_001743553.2:n.9659G>T
(REV3L)
|
|
|
XR_001743555.2:n.9581G>T
(REV3L)
|
|
|
XR_001743556.2:n.9388G>T
(REV3L)
|
|
|
XR_002956293.1:n.10599G>T
(REV3L)
|
|
|
NM_001286431.2:c.8921G>T
(REV3L)
|
NP_001273360.1:p.Gly2974Val
|
|
NM_001372078.1:c.9155G>T
(REV3L)
MANE Select
|
NP_001359007.1:p.Gly3052Val
|
|
NM_001286432.2:c.8921G>T
(REV3L)
|
NP_001273361.1:p.Gly2974Val
|
|
NM_002912.5:c.9155G>T
(REV3L)
|
NP_002903.3:p.Gly3052Val
|
|