ENST00000216185.7:c.387+30A>C
MANE Select
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ENSP00000216185.2:n.387+30A>C
|
|
ENST00000216185.6:c.387+30A>C
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ENSP00000216185.2:n.387+30A>C
|
|
ENST00000403313.5:c.387+30A>C
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ENSP00000385393.1:n.387+30A>C
|
|
ENST00000411915.1:c.387+30A>C
|
ENSP00000409407.1:n.387+30A>C
|
|
ENST00000416967.1:c.81+30A>C
|
ENSP00000469160.1:n.81+30A>C
|
|
ENST00000487725.1:n.367+30A>C
|
|
|
NM_012473.3:c.387+30A>C
|
NP_036605.2:n.387+30A>C
|
|
XM_005261508.1:c.480+30A>C
|
XP_005261565.1:n.480+30A>C
|
|
XM_006724226.1:c.387+30A>C
|
XP_006724289.1:n.387+30A>C
|
|
XM_011530111.1:c.356+3872A>C
|
XP_011528413.1:n.356+3872A>C
|
|
XM_011530111.3:c.356+3872A>C
|
XP_011528413.1:n.356+3872A>C
|
|
NM_012473.4:c.387+30A>C
MANE Select
|
NP_036605.2:n.387+30A>C
|
|