ENST00000324001.8:c.2386G>T
MANE Select
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ENSP00000326018.6:p.Glu796Ter
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ENST00000673881.1:c.1969G>T
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ENSP00000501070.1:p.Glu657Ter
|
|
ENST00000674005.2:c.2671G>T
|
ENSP00000501261.1:p.Glu891Ter
|
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ENST00000674773.1:c.1969G>T
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ENSP00000502579.1:p.Glu657Ter
|
|
ENST00000675517.1:c.2261G>T
|
|
|
ENST00000676076.1:c.2247G>T
|
|
|
ENST00000676260.1:c.2348G>T
|
|
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ENST00000676316.1:c.2273G>T
|
|
|
ENST00000291825.11:c.*2591G>T
|
ENSP00000291825.6:n.*2591G>T
|
|
ENST00000324001.7:c.2386G>T
|
ENSP00000326018.6:p.Glu796Ter
|
|
NM_020956.2:c.*2591G>T , LRG_265t1:c.*2591G>T
|
NP_066007.1:n.*2591G>T
|
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NM_181882.2:c.2386G>T , LRG_265t2:c.2386G>T
|
NP_870998.2:p.Glu796Ter
|
|
XM_011527171.1:c.2386G>T
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XP_011525473.1:p.Glu796Ter
|
|
XM_011527171.2:c.2386G>T
|
XP_011525473.1:p.Glu796Ter
|
|
XM_017027046.1:c.2284G>T
|
XP_016882535.1:p.Glu762Ter
|
|
XM_017027047.1:c.2284G>T
|
XP_016882536.1:p.Glu762Ter
|
|
NM_181882.3:c.2386G>T
MANE Select
|
NP_870998.2:p.Glu796Ter
|
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