ENST00000356518.7:c.*945T>C
MANE Select
|
ENSP00000348912.3:n.*945T>C
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|
ENST00000350009.6:c.*945T>C
|
ENSP00000322550.5:n.*945T>C
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ENST00000356518.6:c.*945T>C
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ENSP00000348912.2:n.*945T>C
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ENST00000379861.8:c.*945T>C
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ENSP00000369190.4:n.*945T>C
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ENST00000466620.5:n.2948T>C
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|
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ENST00000483362.1:n.2310T>C
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|
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ENST00000619289.4:c.*945T>C
|
ENSP00000484600.1:n.*945T>C
|
|
NM_001282447.1:c.*945T>C
|
NP_001269376.1:n.*945T>C
|
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NM_025220.3:c.*945T>C
|
NP_079496.1:n.*945T>C
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|
NM_153202.2:c.*945T>C
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NP_694882.1:n.*945T>C
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|
XM_005260843.1:c.*945T>C
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XP_005260900.1:n.*945T>C
|
|
XM_006723639.1:c.*945T>C
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XP_006723702.1:n.*945T>C
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XM_006723640.1:c.*945T>C
|
XP_006723703.1:n.*945T>C
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XM_011529366.1:c.*945T>C
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XP_011527668.1:n.*945T>C
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|
XM_011529367.1:c.*945T>C
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XP_011527669.1:n.*945T>C
|
|
XM_011529368.1:c.*945T>C
|
XP_011527670.1:n.*945T>C
|
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XM_011529373.1:c.*945T>C
|
XP_011527675.1:n.*945T>C
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|
XR_937153.1:n.3408T>C
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|
|
XR_937154.1:n.3408T>C
|
|
|
XR_937155.1:n.3329T>C
|
|
|
XR_937157.1:n.3331T>C
|
|
|
NM_001282447.2:c.*945T>C
|
NP_001269376.1:n.*945T>C
|
|
NM_025220.4:c.*945T>C
|
NP_079496.1:n.*945T>C
|
|
NM_153202.3:c.*945T>C
|
NP_694882.1:n.*945T>C
|
|
XM_011529373.2:c.*945T>C
|
XP_011527675.1:n.*945T>C
|
|
XR_001754405.1:n.3495T>C
|
|
|
XR_002958534.1:n.3604T>C
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|
|
NM_001282447.3:c.*945T>C
|
NP_001269376.1:n.*945T>C
|
|
NM_025220.5:c.*945T>C
MANE Select
|
NP_079496.1:n.*945T>C
|
|
NM_153202.4:c.*945T>C
|
NP_694882.1:n.*945T>C
|
|