ENST00000267163.6:c.2614C>A
MANE Select
|
ENSP00000267163.4:p.Leu872Met
|
|
ENST00000643064.1:c.194+95351C>A
|
|
|
ENST00000650461.1:c.2614C>A
|
ENSP00000497193.1:p.Leu872Met
|
|
ENST00000267163.4:c.2614C>A
|
ENSP00000267163.4:p.Leu872Met
|
|
ENST00000484879.1:n.348C>A
|
|
|
ENST00000531171.5:n.217C>A
|
|
|
NM_000321.2:c.2614C>A , LRG_517t1:c.2614C>A
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NP_000312.2:p.Leu872Met
|
|
XM_011535171.1:c.2353C>A
|
XP_011533473.1:p.Leu785Met
|
|
XM_011535171.2:c.2353C>A
|
XP_011533473.1:p.Leu785Met
|
|
NM_000321.3:c.2614C>A
MANE Select
|
NP_000312.2:p.Leu872Met
|
|