ENST00000233575.7:c.758A>T
MANE Select
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ENSP00000233575.2:p.Lys253Ile
|
|
ENST00000233575.6:c.758A>T
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ENSP00000233575.2:p.Lys253Ile
|
|
ENST00000427123.5:c.*568A>T
|
ENSP00000405399.1:n.*568A>T
|
|
ENST00000440760.5:c.*603A>T
|
ENSP00000399727.1:n.*603A>T
|
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ENST00000453453.1:c.*285A>T
|
ENSP00000401922.1:n.*285A>T
|
|
ENST00000493711.1:n.475A>T
|
|
|
ENST00000494893.5:n.934A>T
|
|
|
ENST00000537606.5:c.683A>T
|
ENSP00000439208.1:p.Lys228Ile
|
|
NM_001267059.1:c.722A>T
|
NP_001253988.1:p.Lys241Ile
|
|
NM_001267060.1:c.683A>T
|
NP_001253989.1:p.Lys228Ile
|
|
NM_001267061.1:c.698A>T
|
NP_001253990.1:p.Lys233Ile
|
|
NM_014748.3:c.758A>T
|
NP_055563.1:p.Lys253Ile
|
|
NR_049782.1:n.1131A>T
|
|
|
NR_049783.1:n.1104A>T
|
|
|
NR_049784.1:n.1080A>T
|
|
|
NR_049785.1:n.1013A>T
|
|
|
NR_049786.1:n.962A>T
|
|
|
NR_049787.1:n.813A>T
|
|
|
NR_049788.1:n.743A>T
|
|
|
XM_011533203.1:c.116A>T
|
XP_011531505.1:p.Lys39Ile
|
|
XM_011533203.2:c.116A>T
|
XP_011531505.1:p.Lys39Ile
|
|
XM_017005405.2:c.116A>T
|
XP_016860894.1:p.Lys39Ile
|
|
NM_014748.4:c.758A>T
MANE Select
|
NP_055563.1:p.Lys253Ile
|
|
NM_001267059.2:c.722A>T
|
NP_001253988.1:p.Lys241Ile
|
|
NM_001267061.2:c.698A>T
|
NP_001253990.1:p.Lys233Ile
|
|
NR_049782.2:n.1011A>T
|
|
|
NR_049783.2:n.984A>T
|
|
|
NR_049784.2:n.960A>T
|
|
|
NR_049785.2:n.893A>T
|
|
|
NR_049786.2:n.842A>T
|
|
|
NR_049787.2:n.693A>T
|
|
|
NR_049788.2:n.623A>T
|
|
|
NM_001267060.2:c.683A>T
|
NP_001253989.1:p.Lys228Ile
|
|