ENST00000362065.9:c.2403C>T
(FAN1)
MANE Select
|
ENSP00000354497.4:p.Ala801=
|
|
ENST00000562881.2:n.1371C>T
(FAN1)
|
|
|
ENST00000568145.6:n.1279C>T
(FAN1)
|
|
|
ENST00000602886.2:n.2580C>T
(FAN1)
|
|
|
ENST00000654056.1:c.*247C>T
(FAN1)
|
ENSP00000499726.1:n.*247C>T
|
|
ENST00000655421.1:n.3171C>T
(FAN1)
|
|
|
ENST00000656307.1:n.2655C>T
(FAN1)
|
|
|
ENST00000656435.1:c.2403C>T
(FAN1)
|
ENSP00000499534.1:p.Ala801=
|
|
ENST00000657391.1:c.2403C>T
(FAN1)
|
ENSP00000499703.1:p.Ala801=
|
|
ENST00000661974.1:c.1695C>T
(FAN1)
|
|
|
ENST00000664070.1:c.*1943C>T
(FAN1)
|
ENSP00000499478.1:n.*1943C>T
|
|
ENST00000664837.1:c.1113C>T
(FAN1)
|
ENSP00000499780.1:p.Ala371=
|
|
ENST00000667837.1:n.2215C>T
(FAN1)
|
|
|
ENST00000670074.1:c.*1145C>T
(FAN1)
|
ENSP00000499252.1:n.*1145C>T
|
|
ENST00000670849.1:c.2403C>T
(FAN1)
|
ENSP00000499638.1:p.Ala801=
|
|
ENST00000362065.8:c.2403C>T
(FAN1)
|
ENSP00000354497.4:p.Ala801=
|
|
ENST00000565280.5:c.*1244C>T
(FAN1)
|
ENSP00000455573.1:n.*1244C>T
|
|
ENST00000568145.5:n.355C>T
(FAN1)
|
|
|
NM_014967.4:c.2403C>T
(FAN1)
|
NP_055782.3:p.Ala801=
|
|
XM_005254232.3:c.2403C>T
(FAN1)
|
XP_005254289.1:p.Ala801=
|
|
XM_005254234.3:c.2403C>T
(FAN1)
|
XP_005254291.1:p.Ala801=
|
|
XM_005254235.3:c.2403C>T
(FAN1)
|
XP_005254292.1:p.Ala801=
|
|
XM_005254236.2:c.2403C>T
(FAN1)
|
XP_005254293.1:p.Ala801=
|
|
XM_011521370.1:c.1221C>T
(FAN1)
|
XP_011519672.1:p.Ala407=
|
|
XM_011521371.1:c.1218C>T
(FAN1)
|
XP_011519673.1:p.Ala406=
|
|
XM_011521737.1:c.1549-5931G>A
(MTMR10)
|
XP_011520039.1:n.1549-5931G>A
|
|
XM_005254232.4:c.2403C>T
(FAN1)
|
XP_005254289.1:p.Ala801=
|
|
XM_005254234.5:c.2403C>T
(FAN1)
|
XP_005254291.1:p.Ala801=
|
|
XM_011521370.2:c.1221C>T
(FAN1)
|
XP_011519672.1:p.Ala407=
|
|
XM_011521737.3:c.1549-5931G>A
(MTMR10)
|
XP_011520039.1:n.1549-5931G>A
|
|
XM_017022012.2:c.732C>T
(FAN1)
|
XP_016877501.1:p.Ala244=
|
|
XM_017022013.1:c.732C>T
(FAN1)
|
XP_016877502.1:p.Ala244=
|
|
XM_024449874.1:c.1218C>T
(FAN1)
|
XP_024305642.1:p.Ala406=
|
|
XR_001751149.1:n.2702C>T
(FAN1)
|
|
|
XR_001751151.1:n.2698C>T
(FAN1)
|
|
|
NM_014967.5:c.2403C>T
(FAN1)
MANE Select
|
NP_055782.3:p.Ala801=
|
|