ENST00000375708.4:c.442G>T
MANE Select
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ENSP00000364860.3:p.Gly148Cys
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ENST00000375708.3:c.442G>T
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ENSP00000364860.3:p.Gly148Cys
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ENST00000375715.5:c.22G>T
|
ENSP00000364867.1:p.Gly8Cys
|
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ENST00000548585.2:n.172+136G>T
|
|
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ENST00000550066.5:n.910G>T
|
|
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NM_004560.3:c.442G>T
|
NP_004551.2:p.Gly148Cys
|
|
XM_005252008.3:c.22G>T
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XP_005252065.1:p.Gly8Cys
|
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XM_006717121.2:c.22G>T
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XP_006717184.1:p.Gly8Cys
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XM_011518721.1:c.22G>T
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XP_011517023.1:p.Gly8Cys
|
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NM_001318204.1:c.442G>T
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NP_001305133.1:p.Gly148Cys
|
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XM_005252008.4:c.22G>T
|
XP_005252065.1:p.Gly8Cys
|
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XM_006717121.3:c.22G>T
|
XP_006717184.1:p.Gly8Cys
|
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XM_017014762.1:c.433G>T
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XP_016870251.1:p.Gly145Cys
|
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XM_017014763.1:c.22G>T
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XP_016870252.1:p.Gly8Cys
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XR_001746315.1:n.685G>T
|
|
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NM_004560.4:c.442G>T
MANE Select
|
NP_004551.2:p.Gly148Cys
|
|
NM_001318204.2:c.442G>T
|
NP_001305133.1:p.Gly148Cys
|
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