ENST00000647814.1:c.4146+112C>A
MANE Select
|
ENSP00000497274.1:n.4146+112C>A
|
|
ENST00000648523.1:c.34+112C>A
|
|
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ENST00000649459.1:n.494+112C>A
|
|
|
ENST00000370449.8:c.4146+112C>A
|
ENSP00000359478.4:n.4146+112C>A
|
|
NM_000392.4:c.4146+112C>A
|
NP_000383.1:n.4146+112C>A
|
|
XM_006717630.2:c.3450+112C>A
|
XP_006717693.1:n.3450+112C>A
|
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XR_945604.1:n.4276+112C>A
|
|
|
XR_945605.1:n.4210+112C>A
|
|
|
NM_000392.5:c.4146+112C>A
MANE Select
|
NP_000383.2:n.4146+112C>A
|
|
XM_006717630.3:c.3450+112C>A
|
XP_006717693.1:n.3450+112C>A
|
|
XR_945604.3:n.4330+112C>A
|
|
|
XR_945605.3:n.4262+112C>A
|
|
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