ENST00000233575.7:c.788C>G
MANE Select
|
ENSP00000233575.2:p.Ala263Gly
|
|
ENST00000233575.6:c.788C>G
|
ENSP00000233575.2:p.Ala263Gly
|
|
ENST00000427123.5:c.*598C>G
|
ENSP00000405399.1:n.*598C>G
|
|
ENST00000440760.5:c.*633C>G
|
ENSP00000399727.1:n.*633C>G
|
|
ENST00000453453.1:c.*315C>G
|
ENSP00000401922.1:n.*315C>G
|
|
ENST00000493711.1:n.505C>G
|
|
|
ENST00000494893.5:n.964C>G
|
|
|
ENST00000537606.5:c.713C>G
|
ENSP00000439208.1:p.Ala238Gly
|
|
NM_001267059.1:c.752C>G
|
NP_001253988.1:p.Ala251Gly
|
|
NM_001267060.1:c.713C>G
|
NP_001253989.1:p.Ala238Gly
|
|
NM_001267061.1:c.728C>G
|
NP_001253990.1:p.Ala243Gly
|
|
NM_014748.3:c.788C>G
|
NP_055563.1:p.Ala263Gly
|
|
NR_049782.1:n.1161C>G
|
|
|
NR_049783.1:n.1134C>G
|
|
|
NR_049784.1:n.1110C>G
|
|
|
NR_049785.1:n.1043C>G
|
|
|
NR_049786.1:n.992C>G
|
|
|
NR_049787.1:n.843C>G
|
|
|
NR_049788.1:n.773C>G
|
|
|
XM_011533203.1:c.146C>G
|
XP_011531505.1:p.Ala49Gly
|
|
XM_011533203.2:c.146C>G
|
XP_011531505.1:p.Ala49Gly
|
|
XM_017005405.2:c.146C>G
|
XP_016860894.1:p.Ala49Gly
|
|
NM_014748.4:c.788C>G
MANE Select
|
NP_055563.1:p.Ala263Gly
|
|
NM_001267059.2:c.752C>G
|
NP_001253988.1:p.Ala251Gly
|
|
NM_001267061.2:c.728C>G
|
NP_001253990.1:p.Ala243Gly
|
|
NR_049782.2:n.1041C>G
|
|
|
NR_049783.2:n.1014C>G
|
|
|
NR_049784.2:n.990C>G
|
|
|
NR_049785.2:n.923C>G
|
|
|
NR_049786.2:n.872C>G
|
|
|
NR_049787.2:n.723C>G
|
|
|
NR_049788.2:n.653C>G
|
|
|
NM_001267060.2:c.713C>G
|
NP_001253989.1:p.Ala238Gly
|
|