ENST00000324071.10:c.552T=
MANE Select
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ENSP00000324648.2:p.Phe184=
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ENST00000598834.2:c.454T=
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|
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ENST00000324071.8:c.552T=
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ENSP00000324648.2:p.Phe184=
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|
ENST00000593831.1:c.256+2526T=
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ENSP00000470582.1:n.256+2526T=
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|
ENST00000594187.1:n.136T=
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|
|
ENST00000598834.1:n.454T=
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|
|
NM_000767.4:c.552T=
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NP_000758.1:p.Phe184=
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XM_005258569.3:c.552T=
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XP_005258626.1:p.Phe184=
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|
XM_006723050.2:c.552T=
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XP_006723113.1:p.Phe184=
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XM_011526546.1:c.552T=
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XP_011524848.1:p.Phe184=
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|
XM_011526547.1:c.552T=
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XP_011524849.1:p.Phe184=
|
|
XM_011526548.1:c.484+2526T=
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XP_011524850.1:n.484+2526T=
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|
XM_011526549.1:c.-40T=
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XP_011524851.1:n.-40T=
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|
XM_011526550.1:c.364+2526T=
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XP_011524852.1:n.364+2526T=
|
|
NM_000767.5:c.552T=
MANE Select
|
NP_000758.1:p.Phe184=
|
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