ENST00000382103.7:c.*3050G>C
MANE Select
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ENSP00000371535.2:n.*3050G>C
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|
ENST00000680581.1:c.*3430G>C
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ENSP00000506483.1:n.*3430G>C
|
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ENST00000680824.1:n.5772G>C
|
|
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ENST00000681071.1:n.4848G>C
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|
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ENST00000681341.1:n.5603G>C
|
|
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ENST00000681374.1:n.3912G>C
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|
|
ENST00000681948.1:c.*3050G>C
|
ENSP00000505991.1:n.*3050G>C
|
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ENST00000382103.6:c.*3050G>C
|
ENSP00000371535.2:n.*3050G>C
|
|
NM_016955.3:c.*3050G>C
|
NP_058651.3:n.*3050G>C
|
|
XM_005248168.2:c.*3050G>C
|
XP_005248225.1:n.*3050G>C
|
|
XM_006713965.2:c.*3050G>C
|
XP_006714028.1:n.*3050G>C
|
|
XM_011513846.1:c.*3050G>C
|
XP_011512148.1:n.*3050G>C
|
|
XM_011513847.1:c.*3050G>C
|
XP_011512149.1:n.*3050G>C
|
|
XM_011513848.1:c.*3050G>C
|
XP_011512150.1:n.*3050G>C
|
|
XM_011513846.2:c.*3050G>C
|
XP_011512148.1:n.*3050G>C
|
|
XM_011513847.2:c.*3050G>C
|
XP_011512149.1:n.*3050G>C
|
|
XM_017008277.1:c.*3050G>C
|
XP_016863766.1:n.*3050G>C
|
|
XM_017008278.1:c.*3050G>C
|
XP_016863767.1:n.*3050G>C
|
|
NM_016955.4:c.*3050G>C
MANE Select
|
NP_058651.3:n.*3050G>C
|
|