ENST00000233575.7:c.722A>T
MANE Select
|
ENSP00000233575.2:p.Lys241Met
|
|
ENST00000233575.6:c.722A>T
|
ENSP00000233575.2:p.Lys241Met
|
|
ENST00000427123.5:c.*532A>T
|
ENSP00000405399.1:n.*532A>T
|
|
ENST00000440760.5:c.*567A>T
|
ENSP00000399727.1:n.*567A>T
|
|
ENST00000453453.1:c.*249A>T
|
ENSP00000401922.1:n.*249A>T
|
|
ENST00000493711.1:n.439A>T
|
|
|
ENST00000494893.5:n.898A>T
|
|
|
ENST00000537606.5:c.647A>T
|
ENSP00000439208.1:p.Lys216Met
|
|
NM_001267059.1:c.686A>T
|
NP_001253988.1:p.Lys229Met
|
|
NM_001267060.1:c.647A>T
|
NP_001253989.1:p.Lys216Met
|
|
NM_001267061.1:c.662A>T
|
NP_001253990.1:p.Lys221Met
|
|
NM_014748.3:c.722A>T
|
NP_055563.1:p.Lys241Met
|
|
NR_049782.1:n.1095A>T
|
|
|
NR_049783.1:n.1068A>T
|
|
|
NR_049784.1:n.1044A>T
|
|
|
NR_049785.1:n.977A>T
|
|
|
NR_049786.1:n.926A>T
|
|
|
NR_049787.1:n.777A>T
|
|
|
NR_049788.1:n.707A>T
|
|
|
XM_011533203.1:c.80A>T
|
XP_011531505.1:p.Lys27Met
|
|
XM_011533203.2:c.80A>T
|
XP_011531505.1:p.Lys27Met
|
|
XM_017005405.2:c.80A>T
|
XP_016860894.1:p.Lys27Met
|
|
NM_014748.4:c.722A>T
MANE Select
|
NP_055563.1:p.Lys241Met
|
|
NM_001267059.2:c.686A>T
|
NP_001253988.1:p.Lys229Met
|
|
NM_001267061.2:c.662A>T
|
NP_001253990.1:p.Lys221Met
|
|
NR_049782.2:n.975A>T
|
|
|
NR_049783.2:n.948A>T
|
|
|
NR_049784.2:n.924A>T
|
|
|
NR_049785.2:n.857A>T
|
|
|
NR_049786.2:n.806A>T
|
|
|
NR_049787.2:n.657A>T
|
|
|
NR_049788.2:n.587A>T
|
|
|
NM_001267060.2:c.647A>T
|
NP_001253989.1:p.Lys216Met
|
|