ENST00000264381.8:c.621A>G
MANE Select
|
ENSP00000264381.3:p.Gln207=
|
|
ENST00000264381.7:c.621A>G
|
ENSP00000264381.3:p.Gln207=
|
|
ENST00000479451.5:c.107+6901A>G
|
ENSP00000418325.1:n.107+6901A>G
|
|
ENST00000482958.1:c.621A>G
|
ENSP00000419804.1:p.Gln207=
|
|
ENST00000488954.1:c.107+6901A>G
|
ENSP00000418504.1:n.107+6901A>G
|
|
ENST00000497011.5:c.621A>G
|
ENSP00000419505.1:p.Gln207=
|
|
NM_000055.2:c.621A>G
|
NP_000046.1:p.Gln207=
|
|
XM_005247685.1:c.744A>G
|
XP_005247742.1:p.Gln248=
|
|
NM_000055.3:c.621A>G
|
NP_000046.1:p.Gln207=
|
|
NR_137635.1:n.159+6901A>G
|
|
|
NR_137636.1:n.788A>G
|
|
|
NM_000055.4:c.621A>G
MANE Select
|
NP_000046.1:p.Gln207=
|
|
NR_137635.2:n.110+6901A>G
|
|
|
NR_137636.2:n.739A>G
|
|
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