ENST00000334888.10:c.198T>G
|
ENSP00000334844.5:p.Tyr66Ter
|
|
ENST00000544795.6:n.475T>G
|
|
|
ENST00000684926.1:n.214T>G
|
|
|
ENST00000688959.1:c.-62T>G
|
ENSP00000509213.1:n.-62T>G
|
|
ENST00000690736.1:c.198T>G
|
ENSP00000508542.1:p.Tyr66Ter
|
|
ENST00000515837.7:c.198T>G
MANE Select
|
ENSP00000440638.1:p.Tyr66Ter
|
|
ENST00000334888.9:c.198T>G
|
ENSP00000334844.5:p.Tyr66Ter
|
|
ENST00000398979.7:c.15T>G
|
ENSP00000381950.3:p.Tyr5Ter
|
|
ENST00000515837.6:c.198T>G
|
ENSP00000440638.1:p.Tyr66Ter
|
|
ENST00000541473.1:n.212T>G
|
|
|
ENST00000544795.5:n.214T>G
|
|
|
NM_001173990.2:c.198T>G
|
NP_001167461.1:p.Tyr66Ter
|
|
NM_001173991.2:c.198T>G
|
NP_001167462.1:p.Tyr66Ter
|
|
NM_016499.5:c.15T>G
|
NP_057583.2:p.Tyr5Ter
|
|
XM_005274039.3:c.15T>G
|
XP_005274096.1:p.Tyr5Ter
|
|
NM_001330285.1:c.15T>G
|
NP_001317214.1:p.Tyr5Ter
|
|
XM_005274039.4:c.15T>G
|
XP_005274096.1:p.Tyr5Ter
|
|
NM_001173990.3:c.198T>G
MANE Select
|
NP_001167461.1:p.Tyr66Ter
|
|
NM_001173991.3:c.198T>G
|
NP_001167462.1:p.Tyr66Ter
|
|
NM_001330285.2:c.15T>G
|
NP_001317214.1:p.Tyr5Ter
|
|
NM_016499.6:c.15T>G
|
NP_057583.2:p.Tyr5Ter
|
|