ENST00000317447.9:c.1612_1613insT
|
ENSP00000320646.4:p.Arg538MetfsTer28
|
|
ENST00000614302.5:c.1612_1613insT
MANE Select
|
ENSP00000479130.1:p.Arg538MetfsTer28
|
|
ENST00000649953.1:c.1822_1823insT
|
ENSP00000497456.1:p.Arg608MetfsTer28
|
|
ENST00000317447.8:c.1612_1613insT
|
ENSP00000320646.4:p.Arg538MetfsTer28
|
|
ENST00000378345.8:c.817_818insT
|
ENSP00000367596.4:p.Arg273MetfsTer28
|
|
ENST00000406948.7:c.1612_1613insT
|
ENSP00000384627.3:p.Arg538MetfsTer28
|
|
ENST00000535176.1:c.99_100insT
|
|
|
ENST00000537116.5:n.738_739insT
|
|
|
ENST00000537155.1:n.352_353insT
|
|
|
ENST00000542688.5:c.*356_*357insT
|
ENSP00000446281.1:n.*356_*357insT
|
|
ENST00000614302.4:c.1612_1613insT
|
ENSP00000479130.1:p.Arg538MetfsTer28
|
|
NM_001127214.3:c.1612_1613insT
|
NP_001120686.1:p.Arg538MetfsTer28
|
|
NM_001243279.2:c.1612_1613insT
|
NP_001230208.1:p.Arg538MetfsTer28
|
|
NM_001284316.1:c.817_818insT
|
NP_001271245.1:p.Arg273MetfsTer28
|
|
NM_174917.4:c.1612_1613insT
|
NP_777577.2:p.Arg538MetfsTer28
|
|
NR_045667.2:n.738_739insT
|
|
|
NR_104293.1:n.2046_2047insT
|
|
|
XM_005256293.1:c.1612_1613insT
|
XP_005256350.1:p.Arg538MetfsTer?
|
|
XM_011522942.1:c.1612_1613insT
|
XP_011521244.1:p.Arg538MetfsTer?
|
|
XM_011522943.1:c.1612_1613insT
|
XP_011521245.1:p.Arg538MetfsTer?
|
|
XR_933239.1:n.2053_2054insT
|
|
|
XR_933240.1:n.2050_2051insT
|
|
|
XR_933241.1:n.1807_1808insT
|
|
|
NR_147928.1:n.2090_2091insT
|
|
|
NR_147929.1:n.1844_1845insT
|
|
|
XM_005256293.2:c.1612_1613insT
|
XP_005256350.1:p.Arg538MetfsTer?
|
|
XM_017023018.1:c.1612_1613insT
|
XP_016878507.1:p.Arg538MetfsTer?
|
|
XM_017023019.1:c.1612_1613insT
|
XP_016878508.1:p.Arg538MetfsTer16
|
|
XM_017023020.2:c.-3493_-3492insT
|
XP_016878509.1:n.-3493_-3492insT
|
|
XM_017023022.1:c.745_746insT
|
XP_016878511.1:p.Arg249MetfsTer?
|
|
XM_024450186.1:c.817_818insT
|
XP_024305954.1:p.Arg273MetfsTer?
|
|
XM_024450187.1:c.817_818insT
|
XP_024305955.1:p.Arg273MetfsTer28
|
|
XR_001751864.2:n.1859_1860insT
|
|
|
XR_001751865.1:n.1806_1807insT
|
|
|
XR_933240.3:n.2049_2050insT
|
|
|
NM_001127214.4:c.1612_1613insT
|
NP_001120686.1:p.Arg538MetfsTer28
|
|
NM_001243279.3:c.1612_1613insT
MANE Select
|
NP_001230208.1:p.Arg538MetfsTer28
|
|
NM_001284316.2:c.817_818insT
|
NP_001271245.1:p.Arg273MetfsTer28
|
|
NM_174917.5:c.1612_1613insT
|
NP_777577.2:p.Arg538MetfsTer28
|
|
NR_104293.2:n.2003_2004insT
|
|
|
NR_147928.2:n.2047_2048insT
|
|
|
NR_147929.2:n.1801_1802insT
|
|
|