ENST00000374479.4:c.1129_1130delinsGT
MANE Select
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ENSP00000363603.3:p.Val377=
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ENST00000374479.3:c.1129_1130delinsGT
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ENSP00000363603.3:p.Val377=
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|
NM_000147.4:c.1129_1130delinsGT
|
NP_000138.2:p.Val377=
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|
XM_005245821.1:c.754_755delinsGT
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XP_005245878.1:p.Val252=
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|
XM_011541167.1:c.496_497delinsGT
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XP_011539469.1:p.Val166=
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|
XM_005245821.3:c.754_755delinsGT
|
XP_005245878.1:p.Val252=
|
|
XM_011541167.3:c.496_497delinsGT
|
XP_011539469.1:p.Val166=
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|
XM_017000905.2:c.826_827delinsGT
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XP_016856394.1:p.Val276=
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NM_000147.5:c.1129_1130delinsGT
MANE Select
|
NP_000138.2:p.Val377=
|
|
NR_174379.1:n.1307_1308delinsGT
|
|
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NR_174380.1:n.1356_1357delinsGT
|
|
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NR_174381.1:n.1195_1196delinsGT
|
|
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NR_174382.1:n.1592_1593delinsGT
|
|
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