ENST00000375448.4:c.338_339delinsTG
MANE Select
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ENSP00000364597.4:p.Val113=
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|
ENST00000375453.5:c.338_339delinsTG
|
ENSP00000364602.1:p.Val113=
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|
NM_012387.2:c.338_339delinsTG
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NP_036519.2:p.Val113=
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|
XM_011541150.1:c.338_339delinsTG
|
XP_011539452.1:p.Val113=
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|
XM_011541151.1:c.338_339delinsTG
|
XP_011539453.1:p.Val113=
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|
XM_011541152.1:c.-82_-81delinsTG
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XP_011539454.1:n.-82_-81delinsTG
|
|
XM_011541153.1:c.338_339delinsTG
|
XP_011539455.1:p.Val113=
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XM_011541154.1:c.338_339delinsTG
|
XP_011539456.1:p.Val113=
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|
XM_011541155.1:c.338_339delinsTG
|
XP_011539457.1:p.Val113=
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|
XM_011541156.1:c.338_339delinsTG
|
XP_011539458.1:p.Val113=
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|
XM_011541157.1:c.-375_-374delinsTG
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XP_011539459.1:n.-375_-374delinsTG
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|
XM_011541154.2:c.338_339delinsTG
|
XP_011539456.1:p.Val113=
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|
NM_012387.3:c.338_339delinsTG
MANE Select
|
NP_036519.2:p.Val113=
|
|