ENST00000233190.11:c.872+294G>T
MANE Select
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ENSP00000233190.5:n.872+294G>T
|
|
ENST00000233190.10:c.872+294G>T
|
ENSP00000233190.5:n.872+294G>T
|
|
ENST00000423725.5:c.701+294G>T
|
ENSP00000397760.1:n.701+294G>T
|
|
ENST00000432169.5:c.539+294G>T
|
ENSP00000409689.1:n.539+294G>T
|
|
ENST00000440274.5:c.764+294G>T
|
ENSP00000409766.1:n.764+294G>T
|
|
ENST00000449699.5:c.872+294G>T
|
ENSP00000399912.1:n.872+294G>T
|
|
ENST00000455934.6:c.914+294G>T
|
ENSP00000392709.2:n.914+294G>T
|
|
ENST00000457011.5:c.524+294G>T
|
ENSP00000400976.1:n.524+294G>T
|
|
NM_001199981.1:c.764+294G>T
|
NP_001186910.1:n.764+294G>T
|
|
NM_001199982.1:c.539+294G>T
|
NP_001186911.1:n.539+294G>T
|
|
NM_001199983.1:c.701+294G>T
|
NP_001186912.1:n.701+294G>T
|
|
NM_001199984.1:c.914+294G>T
|
NP_001186913.1:n.914+294G>T
|
|
NM_005006.6:c.872+294G>T
|
NP_004997.4:n.872+294G>T
|
|
XM_017004188.2:c.113+294G>T
|
XP_016859677.1:n.113+294G>T
|
|
NM_001199981.2:c.764+294G>T
|
NP_001186910.1:n.764+294G>T
|
|
NM_001199982.2:c.539+294G>T
|
NP_001186911.1:n.539+294G>T
|
|
NM_001199983.2:c.701+294G>T
|
NP_001186912.1:n.701+294G>T
|
|
NM_005006.7:c.872+294G>T
MANE Select
|
NP_004997.4:n.872+294G>T
|
|
NM_001199984.2:c.914+294G>T
|
NP_001186913.1:n.914+294G>T
|
|