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ENST00000405460.9:c.10065_10068delinsCATT
MANE Select
|
ENSP00000384582.2:p.Ile3355=
|
|
|
ENST00000639431.1:c.265+49351_265+49354delinsCATT
|
ENSP00000491057.1:n.265+49351_265+49354de...
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|
|
ENST00000640374.1:n.3209_3212delinsCATT
|
|
|
|
ENST00000640464.1:n.484_487delinsCATT
|
|
|
|
ENST00000405460.6:c.10065_10068delinsCATT
|
ENSP00000384582.2:p.Ile3355=
|
|
|
ENST00000509621.1:c.2762_2765delinsCATT
|
|
|
|
NM_032119.3:c.10065_10068delinsCATT
|
NP_115495.3:p.Ile3355=
|
|
|
NR_003149.1:n.10078_10081delinsCATT
|
|
|
|
XM_011543675.1:c.10062_10065delinsCATT
|
XP_011541977.1:p.Ile3354=
|
|
|
XM_011543676.1:c.9984_9987delinsCATT
|
XP_011541978.1:p.Ile3328=
|
|
|
XM_011543677.1:c.7368_7371delinsCATT
|
XP_011541979.1:p.Ile2456=
|
|
|
XM_011543678.1:c.10065_10068delinsCATT
|
XP_011541980.1:p.Ile3355=
|
|
|
XM_011543679.1:c.10065_10068delinsCATT
|
XP_011541981.1:p.Ile3355=
|
|
|
XR_948560.1:n.272-9754_272-9751delinsAATG
|
|
|
|
NM_032119.4:c.10065_10068delinsCATT
MANE Select
|
NP_115495.3:p.Ile3355=
|
|
|
XM_017009963.2:c.10086_10089delinsCATT
|
XP_016865452.1:p.Ile3362=
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|
|
XM_017009964.2:c.10083_10086delinsCATT
|
XP_016865453.1:p.Ile3361=
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|
|
XM_017009965.1:c.10083_10086delinsCATT
|
XP_016865454.1:p.Ile3361=
|
|
|
XM_017009966.2:c.10005_10008delinsCATT
|
XP_016865455.1:p.Ile3335=
|
|
|
XM_017009967.1:c.9990_9993delinsCATT
|
XP_016865456.1:p.Ile3330=
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|
|
XM_017009968.2:c.10086_10089delinsCATT
|
XP_016865457.1:p.Ile3362=
|
|
|
XM_017009969.2:c.10086_10089delinsCATT
|
XP_016865458.1:p.Ile3362=
|
|
|
XM_017009970.2:c.10086_10089delinsCATT
|
XP_016865459.1:p.Ile3362=
|
|
|
XM_017009971.2:c.10086_10089delinsCATT
|
XP_016865460.1:p.Ile3362=
|
|
|
XM_017009972.1:c.3204_3207delinsCATT
|
XP_016865461.1:p.Ile1068=
|
|
|
XM_017009973.1:c.3183_3186delinsCATT
|
XP_016865462.1:p.Ile1061=
|
|
|
XM_017009974.2:c.10086_10089delinsCATT
|
XP_016865463.1:p.Ile3362=
|
|
|
XR_001742802.1:n.2523-9754_2523-9751delinsAATG
|
|
|
|
NR_003149.2:n.10081_10084delinsCATT
|
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