ENST00000260197.12:c.3460+912A>G
MANE Select
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ENSP00000260197.6:n.3460+912A>G
|
|
ENST00000260197.11:c.3460+912A>G
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ENSP00000260197.6:n.3460+912A>G
|
|
ENST00000525532.5:c.292+912A>G
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ENSP00000434634.1:n.292+912A>G
|
|
NM_003105.5:c.3460+912A>G
|
NP_003096.1:n.3460+912A>G
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|
XM_011542963.1:c.3346+912A>G
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XP_011541265.1:n.3346+912A>G
|
|
XM_011542964.1:c.3460+912A>G
|
XP_011541266.1:n.3460+912A>G
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|
XM_011542965.1:c.1921+912A>G
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XP_011541267.1:n.1921+912A>G
|
|
XM_011542966.1:c.820+912A>G
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XP_011541268.1:n.820+912A>G
|
|
XM_011542967.1:c.292+912A>G
|
XP_011541269.1:n.292+912A>G
|
|
XM_011542963.3:c.3346+912A>G
|
XP_011541265.1:n.3346+912A>G
|
|
XM_011542965.3:c.1921+912A>G
|
XP_011541267.1:n.1921+912A>G
|
|
XM_011542967.3:c.292+912A>G
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XP_011541269.1:n.292+912A>G
|
|
XM_017018169.2:c.3148+912A>G
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XP_016873658.1:n.3148+912A>G
|
|
XM_017018170.2:c.2935+912A>G
|
XP_016873659.1:n.2935+912A>G
|
|
XM_017018171.1:c.3460+912A>G
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XP_016873660.1:n.3460+912A>G
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|
XM_017018172.2:c.820+912A>G
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XP_016873661.1:n.820+912A>G
|
|
NM_003105.6:c.3460+912A>G
MANE Select
|
NP_003096.2:n.3460+912A>G
|
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