ENST00000324001.8:c.2186T>A
MANE Select
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ENSP00000326018.6:p.Leu729His
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ENST00000673881.1:c.1769T>A
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ENSP00000501070.1:p.Leu590His
|
|
ENST00000674005.2:c.2471T>A
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ENSP00000501261.1:p.Leu824His
|
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ENST00000674773.1:c.1769T>A
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ENSP00000502579.1:p.Leu590His
|
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ENST00000675517.1:c.2061T>A
|
|
|
ENST00000676076.1:c.2047T>A
|
|
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ENST00000676260.1:c.2148T>A
|
|
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ENST00000676316.1:c.2073T>A
|
|
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ENST00000291825.11:c.*2391T>A
|
ENSP00000291825.6:n.*2391T>A
|
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ENST00000324001.7:c.2186T>A
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ENSP00000326018.6:p.Leu729His
|
|
NM_020956.2:c.*2391T>A , LRG_265t1:c.*2391T>A
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NP_066007.1:n.*2391T>A
|
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NM_181882.2:c.2186T>A , LRG_265t2:c.2186T>A
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NP_870998.2:p.Leu729His
|
|
XM_011527171.1:c.2186T>A
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XP_011525473.1:p.Leu729His
|
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XM_011527171.2:c.2186T>A
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XP_011525473.1:p.Leu729His
|
|
XM_017027046.1:c.2084T>A
|
XP_016882535.1:p.Leu695His
|
|
XM_017027047.1:c.2084T>A
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XP_016882536.1:p.Leu695His
|
|
NM_181882.3:c.2186T>A
MANE Select
|
NP_870998.2:p.Leu729His
|
|