ENST00000321612.8:c.2052+2T>C
MANE Select
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ENSP00000370737.4:n.2052+2T>C
|
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ENST00000460457.2:n.212+2T>C
|
|
|
ENST00000638233.1:n.487+2T>C
|
|
|
ENST00000638661.1:c.252+2T>C
|
ENSP00000491369.1:n.252+2T>C
|
|
ENST00000638694.1:n.239+2T>C
|
|
|
ENST00000639318.1:c.252+2T>C
|
ENSP00000491932.1:n.252+2T>C
|
|
ENST00000639364.1:n.1752+2T>C
|
|
|
ENST00000639443.1:n.1620+2T>C
|
|
|
ENST00000639954.1:n.1760+2T>C
|
|
|
ENST00000640208.1:c.254T>C
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ENSP00000491895.1:p.Val85Ala
|
|
ENST00000640505.1:n.291+2T>C
|
|
|
ENST00000640592.1:n.1937T>C
|
|
|
ENST00000321612.6:c.2052+2T>C
|
ENSP00000370737.3:n.2052+2T>C
|
|
ENST00000460457.1:n.193T>C
|
|
|
NM_000170.2:c.2052+2T>C , LRG_643t1:c.2052+2T>C
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NP_000161.2:n.2052+2T>C
|
|
NM_000170.3:c.2052+2T>C
MANE Select
|
NP_000161.2:n.2052+2T>C
|
|