|
NM_006885.4:c.2915C>T
MANE Select
|
NP_008816.3:p.Ser972Leu
|
|
ENST00000268489.10:c.2915C>T
MANE Select
|
ENSP00000268489.5:p.Ser972Leu
|
|
NM_001164766.1:c.173C>T
|
NP_001158238.1:p.Ser58Leu
|
|
NM_001164766.2:c.173C>T
|
NP_001158238.1:p.Ser58Leu
|
|
NM_001386735.1:c.2915C>T
|
NP_001373664.1:p.Ser972Leu
|
|
NM_006885.3:c.2915C>T
|
NP_008816.3:p.Ser972Leu
|
|
ENST00000268489.9:c.2915C>T
|
ENSP00000268489.5:p.Ser972Leu
|
|
ENST00000397992.5:c.173C>T
|
ENSP00000438926.3:p.Ser58Leu
|
|
ENST00000641206.2:c.2915C>T
|
ENSP00000493252.1:p.Ser972Leu
|
|
XM_005255957.2:c.2915C>T
|
XP_005256014.1:p.Ser972Leu
|
|
XM_005255957.4:c.2915C>T
|
XP_005256014.1:p.Ser972Leu
|
|
XM_017023251.2:c.266C>T
|
XP_016878740.1:p.Ser89Leu
|
|
XM_024450291.1:c.266C>T
|
XP_024306059.1:p.Ser89Leu
|