ENST00000281928.9:c.2683T>G
MANE Select
|
ENSP00000281928.3:p.Leu895Val
|
|
ENST00000548743.2:c.2653T>G
|
ENSP00000448553.2:p.Leu885Val
|
|
ENST00000549786.2:c.2111T>G
|
|
|
ENST00000647927.1:n.3056T>G
|
|
|
ENST00000648173.1:n.1478T>G
|
|
|
ENST00000648379.1:n.1051T>G
|
|
|
ENST00000648737.1:n.2447T>G
|
|
|
ENST00000648916.1:n.694T>G
|
|
|
ENST00000649607.1:c.867T>G
|
|
|
ENST00000650226.1:c.2683T>G
|
ENSP00000496981.1:p.Leu895Val
|
|
ENST00000281928.7:c.2683T>G
|
ENSP00000281928.3:p.Leu895Val
|
|
NM_015335.4:c.2683T>G
|
NP_056150.1:p.Leu895Val
|
|
XM_011538080.1:c.2683T>G
|
XP_011536382.1:p.Leu895Val
|
|
XM_011538081.1:c.2680T>G
|
XP_011536383.1:p.Leu894Val
|
|
XM_011538082.1:c.2653T>G
|
XP_011536384.1:p.Leu885Val
|
|
XM_011538080.2:c.2683T>G
|
XP_011536382.1:p.Leu895Val
|
|
XM_011538081.2:c.2680T>G
|
XP_011536383.1:p.Leu894Val
|
|
XM_011538082.2:c.2653T>G
|
XP_011536384.1:p.Leu885Val
|
|
XM_017019090.1:c.2680T>G
|
XP_016874579.1:p.Leu894Val
|
|
NM_015335.5:c.2683T>G
MANE Select
|
NP_056150.1:p.Leu895Val
|
|