ENST00000368802.8:c.9153T>C
(REV3L)
MANE Select
|
ENSP00000357792.3:p.His3051=
|
|
ENST00000666581.2:n.277+29302A>G
(MFSD4B)
|
|
|
ENST00000673245.1:n.273+11685A>G
(MFSD4B)
|
|
|
ENST00000673446.1:n.179+39623A>G
(MFSD4B)
|
|
|
ENST00000358835.7:c.9153T>C
(REV3L)
|
ENSP00000351697.3:p.His3051=
|
|
ENST00000368802.7:c.9153T>C
(REV3L)
|
ENSP00000357792.3:p.His3051=
|
|
ENST00000368805.5:c.9153T>C
(REV3L)
|
ENSP00000357795.1:p.His3051=
|
|
ENST00000422377.5:c.*9137T>C
(REV3L)
|
ENSP00000393184.1:n.*9137T>C
|
|
ENST00000434009.5:c.*9244T>C
(REV3L)
|
ENSP00000391605.1:n.*9244T>C
|
|
ENST00000435970.5:c.8919T>C
(REV3L)
|
ENSP00000402003.1:p.His2973=
|
|
ENST00000462119.5:n.1290T>C
(REV3L)
|
|
|
NM_001286431.1:c.8919T>C
(REV3L)
|
NP_001273360.1:p.His2973=
|
|
NM_001286432.1:c.8919T>C
(REV3L)
|
NP_001273361.1:p.His2973=
|
|
NM_002912.4:c.9153T>C
(REV3L)
|
NP_002903.3:p.His3051=
|
|
XM_006715543.2:c.9153T>C
(REV3L)
|
XP_006715606.1:p.His3051=
|
|
XM_006715544.2:c.8919T>C
(REV3L)
|
XP_006715607.1:p.His2973=
|
|
XM_011536028.1:c.9234T>C
(REV3L)
|
XP_011534330.1:p.His3078=
|
|
XM_011536029.1:c.9231T>C
(REV3L)
|
XP_011534331.1:p.His3077=
|
|
XM_011536030.1:c.9156T>C
(REV3L)
|
XP_011534332.1:p.His3052=
|
|
XM_011536031.1:c.9000T>C
(REV3L)
|
XP_011534333.1:p.His3000=
|
|
XM_011536032.1:c.9000T>C
(REV3L)
|
XP_011534334.1:p.His3000=
|
|
XR_942871.1:n.2045+29302A>G
|
|
|
XM_011536028.2:c.9234T>C
(REV3L)
|
XP_011534330.1:p.His3078=
|
|
XM_011536029.3:c.9231T>C
(REV3L)
|
XP_011534331.1:p.His3077=
|
|
XM_011536030.3:c.9156T>C
(REV3L)
|
XP_011534332.1:p.His3052=
|
|
XM_011536031.3:c.9000T>C
(REV3L)
|
XP_011534333.1:p.His3000=
|
|
XM_011536032.2:c.9000T>C
(REV3L)
|
XP_011534334.1:p.His3000=
|
|
XM_017011152.2:c.8997T>C
(REV3L)
|
XP_016866641.1:p.His2999=
|
|
XM_017011153.1:c.8997T>C
(REV3L)
|
XP_016866642.1:p.His2999=
|
|
XM_017011154.1:c.8997T>C
(REV3L)
|
XP_016866643.1:p.His2999=
|
|
XR_001743550.2:n.9339T>C
(REV3L)
|
|
|
XR_001743552.2:n.9261T>C
(REV3L)
|
|
|
XR_001743553.2:n.9657T>C
(REV3L)
|
|
|
XR_001743555.2:n.9579T>C
(REV3L)
|
|
|
XR_001743556.2:n.9386T>C
(REV3L)
|
|
|
XR_002956293.1:n.10597T>C
(REV3L)
|
|
|
NM_001286431.2:c.8919T>C
(REV3L)
|
NP_001273360.1:p.His2973=
|
|
NM_001372078.1:c.9153T>C
(REV3L)
MANE Select
|
NP_001359007.1:p.His3051=
|
|
NM_001286432.2:c.8919T>C
(REV3L)
|
NP_001273361.1:p.His2973=
|
|
NM_002912.5:c.9153T>C
(REV3L)
|
NP_002903.3:p.His3051=
|
|