ENST00000265631.10:c.1841+111_1841+112delinsGA
MANE Select
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ENSP00000265631.6:n.1841+111_1841+112delinsGA
|
|
ENST00000265631.9:c.1841+111_1841+112delinsGA
|
ENSP00000265631.5:n.1841+111_1841+112delinsGA
|
|
ENST00000416240.6:c.1844+111_1844+112delinsGA
|
ENSP00000400101.2:n.1844+111_1844+112delinsGA
|
|
ENST00000494085.1:n.344+111_344+112delinsGA
|
|
|
NM_001160210.1:c.1844+111_1844+112delinsGA
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NP_001153682.1:n.1844+111_1844+112delinsGA
|
|
NM_014251.2:c.1841+111_1841+112delinsGA
|
NP_055066.1:n.1841+111_1841+112delinsGA
|
|
NR_027662.1:n.1916+111_1916+112delinsGA
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|
|
XM_006715831.2:c.1874+111_1874+112delinsGA
|
XP_006715894.1:n.1874+111_1874+112delinsGA
|
|
XM_011515728.1:c.989+111_989+112delinsGA
|
XP_011514030.1:n.989+111_989+112delinsGA
|
|
XM_006715831.4:c.1874+111_1874+112delinsGA
|
XP_006715894.1:n.1874+111_1874+112delinsGA
|
|
XM_017011663.1:c.1832+111_1832+112delinsGA
|
XP_016867152.1:n.1832+111_1832+112delinsGA
|
|
XM_017011664.2:c.989+111_989+112delinsGA
|
XP_016867153.1:n.989+111_989+112delinsGA
|
|
XM_017011665.1:c.989+111_989+112delinsGA
|
XP_016867154.1:n.989+111_989+112delinsGA
|
|
XR_001744525.2:n.2087+111_2087+112delinsGA
|
|
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XR_002956405.1:n.2645+111_2645+112delinsGA
|
|
|
NM_014251.3:c.1841+111_1841+112delinsGA
MANE Select
|
NP_055066.1:n.1841+111_1841+112delinsGA
|
|
NR_027662.2:n.1867+111_1867+112delinsGA
|
|
|
NM_001160210.2:c.1844+111_1844+112delinsGA
|
NP_001153682.1:n.1844+111_1844+112delinsGA
|
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