ENST00000405460.9:c.11489C>A
MANE Select
|
ENSP00000384582.2:p.Ala3830Asp
|
|
ENST00000425867.3:c.620C>A
|
ENSP00000392618.3:p.Ala207Asp
|
|
ENST00000639431.1:c.265+78885C>A
|
ENSP00000491057.1:n.265+78885C>A
|
|
ENST00000640374.1:n.4633C>A
|
|
|
ENST00000640464.1:n.1908C>A
|
|
|
ENST00000405460.6:c.11489C>A
|
ENSP00000384582.2:p.Ala3830Asp
|
|
ENST00000509621.1:c.4186C>A
|
|
|
NM_032119.3:c.11489C>A
|
NP_115495.3:p.Ala3830Asp
|
|
NR_003149.1:n.11502C>A
|
|
|
XM_011543675.1:c.11486C>A
|
XP_011541977.1:p.Ala3829Asp
|
|
XM_011543676.1:c.11408C>A
|
XP_011541978.1:p.Ala3803Asp
|
|
XM_011543677.1:c.8792C>A
|
XP_011541979.1:p.Ala2931Asp
|
|
XM_011543678.1:c.11489C>A
|
XP_011541980.1:p.Ala3830Asp
|
|
NM_032119.4:c.11489C>A
MANE Select
|
NP_115495.3:p.Ala3830Asp
|
|
XM_017009963.2:c.11510C>A
|
XP_016865452.1:p.Ala3837Asp
|
|
XM_017009964.2:c.11507C>A
|
XP_016865453.1:p.Ala3836Asp
|
|
XM_017009965.1:c.11507C>A
|
XP_016865454.1:p.Ala3836Asp
|
|
XM_017009966.2:c.11429C>A
|
XP_016865455.1:p.Ala3810Asp
|
|
XM_017009967.1:c.11414C>A
|
XP_016865456.1:p.Ala3805Asp
|
|
XM_017009968.2:c.11510C>A
|
XP_016865457.1:p.Ala3837Asp
|
|
XM_017009969.2:c.11510C>A
|
XP_016865458.1:p.Ala3837Asp
|
|
XM_017009970.2:c.11510C>A
|
XP_016865459.1:p.Ala3837Asp
|
|
XM_017009971.2:c.11510C>A
|
XP_016865460.1:p.Ala3837Asp
|
|
XM_017009972.1:c.4628C>A
|
XP_016865461.1:p.Ala1543Asp
|
|
XM_017009973.1:c.4607C>A
|
XP_016865462.1:p.Ala1536Asp
|
|
NR_003149.2:n.11505C>A
|
|
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