|
ENST00000368802.8:c.9057C>T
(REV3L)
MANE Select
|
ENSP00000357792.3:p.Thr3019=
|
|
|
ENST00000666581.2:n.277+29398G>A
(MFSD4B)
|
|
|
|
ENST00000673245.1:n.273+11781G>A
(MFSD4B)
|
|
|
|
ENST00000673446.1:n.179+39719G>A
(MFSD4B)
|
|
|
|
ENST00000358835.7:c.9057C>T
(REV3L)
|
ENSP00000351697.3:p.Thr3019=
|
|
|
ENST00000368802.7:c.9057C>T
(REV3L)
|
ENSP00000357792.3:p.Thr3019=
|
|
|
ENST00000368805.5:c.9057C>T
(REV3L)
|
ENSP00000357795.1:p.Thr3019=
|
|
|
ENST00000422377.5:c.*9041C>T
(REV3L)
|
ENSP00000393184.1:n.*9041C>T
|
|
|
ENST00000434009.5:c.*9148C>T
(REV3L)
|
ENSP00000391605.1:n.*9148C>T
|
|
|
ENST00000435970.5:c.8823C>T
(REV3L)
|
ENSP00000402003.1:p.Thr2941=
|
|
|
ENST00000462119.5:n.1194C>T
(REV3L)
|
|
|
|
NM_001286431.1:c.8823C>T
(REV3L)
|
NP_001273360.1:p.Thr2941=
|
|
|
NM_001286432.1:c.8823C>T
(REV3L)
|
NP_001273361.1:p.Thr2941=
|
|
|
NM_002912.4:c.9057C>T
(REV3L)
|
NP_002903.3:p.Thr3019=
|
|
|
XM_006715543.2:c.9057C>T
(REV3L)
|
XP_006715606.1:p.Thr3019=
|
|
|
XM_006715544.2:c.8823C>T
(REV3L)
|
XP_006715607.1:p.Thr2941=
|
|
|
XM_011536028.1:c.9138C>T
(REV3L)
|
XP_011534330.1:p.Thr3046=
|
|
|
XM_011536029.1:c.9135C>T
(REV3L)
|
XP_011534331.1:p.Thr3045=
|
|
|
XM_011536030.1:c.9060C>T
(REV3L)
|
XP_011534332.1:p.Thr3020=
|
|
|
XM_011536031.1:c.8904C>T
(REV3L)
|
XP_011534333.1:p.Thr2968=
|
|
|
XM_011536032.1:c.8904C>T
(REV3L)
|
XP_011534334.1:p.Thr2968=
|
|
|
XR_942871.1:n.2045+29398G>A
|
|
|
|
XM_011536028.2:c.9138C>T
(REV3L)
|
XP_011534330.1:p.Thr3046=
|
|
|
XM_011536029.3:c.9135C>T
(REV3L)
|
XP_011534331.1:p.Thr3045=
|
|
|
XM_011536030.3:c.9060C>T
(REV3L)
|
XP_011534332.1:p.Thr3020=
|
|
|
XM_011536031.3:c.8904C>T
(REV3L)
|
XP_011534333.1:p.Thr2968=
|
|
|
XM_011536032.2:c.8904C>T
(REV3L)
|
XP_011534334.1:p.Thr2968=
|
|
|
XM_017011152.2:c.8901C>T
(REV3L)
|
XP_016866641.1:p.Thr2967=
|
|
|
XM_017011153.1:c.8901C>T
(REV3L)
|
XP_016866642.1:p.Thr2967=
|
|
|
XM_017011154.1:c.8901C>T
(REV3L)
|
XP_016866643.1:p.Thr2967=
|
|
|
XR_001743550.2:n.9243C>T
(REV3L)
|
|
|
|
XR_001743552.2:n.9165C>T
(REV3L)
|
|
|
|
XR_001743553.2:n.9561C>T
(REV3L)
|
|
|
|
XR_001743555.2:n.9483C>T
(REV3L)
|
|
|
|
XR_001743556.2:n.9290C>T
(REV3L)
|
|
|
|
XR_002956293.1:n.10501C>T
(REV3L)
|
|
|
|
NM_001286431.2:c.8823C>T
(REV3L)
|
NP_001273360.1:p.Thr2941=
|
|
|
NM_001372078.1:c.9057C>T
(REV3L)
MANE Select
|
NP_001359007.1:p.Thr3019=
|
|
|
NM_001286432.2:c.8823C>T
(REV3L)
|
NP_001273361.1:p.Thr2941=
|
|
|
NM_002912.5:c.9057C>T
(REV3L)
|
NP_002903.3:p.Thr3019=
|
|
