ENST00000687160.1:c.788T>G
MANE Select
|
ENSP00000510345.1:p.Val263Gly
|
|
ENST00000264260.6:c.788T>G
|
ENSP00000264260.2:p.Val263Gly
|
|
ENST00000409369.1:c.362T>G
|
ENSP00000387201.1:p.Val121Gly
|
|
NM_003853.3:c.788T>G
|
NP_003844.1:p.Val263Gly
|
|
XM_011512087.1:c.362T>G
|
XP_011510389.1:p.Val121Gly
|
|
XM_011512088.1:c.362T>G
|
XP_011510390.1:p.Val121Gly
|
|
XM_011512089.1:c.788T>G
|
XP_011510391.1:p.Val263Gly
|
|
XR_923052.1:n.1125T>G
|
|
|
XM_011512087.2:c.362T>G
|
XP_011510389.1:p.Val121Gly
|
|
XM_011512088.2:c.362T>G
|
XP_011510390.1:p.Val121Gly
|
|
XM_024453197.1:c.788T>G
|
XP_024308965.1:p.Val263Gly
|
|
XM_024453198.1:c.788T>G
|
XP_024308966.1:p.Val263Gly
|
|
XM_024453199.1:c.788T>G
|
XP_024308967.1:p.Val263Gly
|
|
XM_024453200.1:c.788T>G
|
XP_024308968.1:p.Val263Gly
|
|
XM_024453201.1:c.788T>G
|
XP_024308969.1:p.Val263Gly
|
|
XR_001739011.2:n.1123T>G
|
|
|
NM_001393486.1:c.788T>G
|
NP_001380415.1:p.Val263Gly
|
|
NM_001393487.1:c.788T>G
MANE Select
|
NP_001380416.1:p.Val263Gly
|
|
NM_001393488.1:c.362T>G
|
NP_001380417.1:p.Val121Gly
|
|
NM_001393489.1:c.362T>G
|
NP_001380418.1:p.Val121Gly
|
|
NM_003853.4:c.788T>G
|
NP_003844.1:p.Val263Gly
|
|