ENST00000334888.10:c.138T>A
|
ENSP00000334844.5:p.Gly46=
|
|
ENST00000544795.6:n.415T>A
|
|
|
ENST00000684926.1:n.154T>A
|
|
|
ENST00000688959.1:c.-122T>A
|
ENSP00000509213.1:n.-122T>A
|
|
ENST00000690736.1:c.138T>A
|
ENSP00000508542.1:p.Gly46=
|
|
ENST00000515837.7:c.138T>A
MANE Select
|
ENSP00000440638.1:p.Gly46=
|
|
ENST00000334888.9:c.138T>A
|
ENSP00000334844.5:p.Gly46=
|
|
ENST00000398979.7:c.-46T>A
|
ENSP00000381950.3:n.-46T>A
|
|
ENST00000515837.6:c.138T>A
|
ENSP00000440638.1:p.Gly46=
|
|
ENST00000541473.1:n.152T>A
|
|
|
ENST00000544795.5:n.154T>A
|
|
|
NM_001173990.2:c.138T>A
|
NP_001167461.1:p.Gly46=
|
|
NM_001173991.2:c.138T>A
|
NP_001167462.1:p.Gly46=
|
|
NM_016499.5:c.-46T>A
|
NP_057583.2:n.-46T>A
|
|
XM_005274039.3:c.-46T>A
|
XP_005274096.1:n.-46T>A
|
|
NM_001330285.1:c.-46T>A
|
NP_001317214.1:n.-46T>A
|
|
XM_005274039.4:c.-46T>A
|
XP_005274096.1:n.-46T>A
|
|
NM_001173990.3:c.138T>A
MANE Select
|
NP_001167461.1:p.Gly46=
|
|
NM_001173991.3:c.138T>A
|
NP_001167462.1:p.Gly46=
|
|
NM_001330285.2:c.-46T>A
|
NP_001317214.1:n.-46T>A
|
|
NM_016499.6:c.-46T>A
|
NP_057583.2:n.-46T>A
|
|