ENST00000248633.9:c.2164del
MANE Select
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ENSP00000248633.4:p.Val723PhefsTer?
|
|
ENST00000248633.8:c.2164del
|
ENSP00000248633.4:p.Val723PhefsTer?
|
|
ENST00000428214.5:c.1993del
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ENSP00000394413.1:p.Val666PhefsTer?
|
|
ENST00000438045.5:c.1198del
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ENSP00000410438.1:p.Val401PhefsTer?
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ENST00000484913.5:n.2203del
|
|
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ENST00000496420.5:n.1840del
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|
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NM_000466.2:c.2164del
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NP_000457.1:p.Val723PhefsTer?
|
|
NM_001282677.1:c.1993del
|
NP_001269606.1:p.Val666PhefsTer?
|
|
NM_001282678.1:c.1540del
|
NP_001269607.1:p.Val515PhefsTer?
|
|
XM_005250433.3:c.415del
|
XP_005250490.1:p.Val140PhefsTer?
|
|
XR_242246.3:n.2260del
|
|
|
XM_017012319.2:c.415del
|
XP_016867808.1:p.Val140PhefsTer?
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|
XR_001744808.2:n.1191del
|
|
|
XR_242246.5:n.2211del
|
|
|
NM_000466.3:c.2164del
MANE Select
|
NP_000457.1:p.Val723PhefsTer?
|
|
NM_001282677.2:c.1993del
|
NP_001269606.1:p.Val666PhefsTer?
|
|
NM_001282678.2:c.1540del
|
NP_001269607.1:p.Val515PhefsTer?
|
|